List of compounds with carbon number 8

Last updated

This is a partial list of molecules that contain 8 carbon atoms.

Chemical formula Synonyms CAS number
C8ClF15O perfluorooctanoyl chloride 335-64-8
C8Cl4N2 tetrachloroisophthalonitrile 1897-45-6
C8Co2O8 dicobalt octacarbonyl 10210-68-1
C8F4N2 tetrafluorophthalonitrile 1835-65-0
C8F14O3 heptafluorobutyric anhydride 336-59-4
C8F16 perfluoroethylcyclohexane 335-21-7
C8F17I perfluorooctyl iodide 507-63-1
C8F18 perfluorooctane 307-34-6
C8H(NO2)7 heptanitrocubane 99393-62-1
C8H2Cl4O2 fthalide 27355-22-2
C8H2F4O4 tetrafluorophthalic acid 652-03-9
C8H3Cl5O2 pentachlorophenyl acetate 1441-02-7
C8H4FeO4 cyclobutadienecarboxaldehydeiron tricarbonyl 33056-62-1
C8H4N2 phthalonitrile 91-15-6
C8H4N2S2 bitoscanate 4044-65-9
C8H4O3 phthalic anhydride 85-44-9
C8H5Ag silver phenylacetylenide 33440-88-9
C8H5BrMoO3 cyclopentadienylmolybdenumtricarbonyl bromide 12079-79-7
C8H5Cl5 pentachloroethylbenzene 606-07-5
C8H5CrO3 cyclopentadienylchromium tricarbonyl 12079-91-3
C8H5Cu copper phenylacetylenide 13146-23-1
C8H5F5O pentafluoroethoxybenzene 1644-22-0
C8H5MnO2S cyclopentadienylmanganesedicarbonylthiocarbonyl 31741-76-1
C8H5NOS benzoyl isothiocyanate 532-55-8
C8H5NO2 isatin 91-56-5
C8H5NO2 phthalimide 85-41-6
C8H5NO3 isatoic anhydride 118-48-9
C8H5N3 pyridinium dicyanomethylide 27032-01-5
C8H6 cubene radical 77478-10-5
C8H6 cyclooctatrienyne radical 4514-69-6
C8H6 phenylacetylene 536-74-3
C8H6Cl3NO3 triclopyr methyl ester 60825-26-5
C8H6Cl4O2 tetrachloroveratrole 944-61-6
C8H6N2 cinnoline 253-66-7
C8H6N2 phthalazine 253-52-1
C8H6N2 quinazo
C8H6N2 quinoxaline 91-19-0
C8H6N2O phenylfurazan 10349-06-1
C8H6N2O2 quindoxin 2423-66-7
C8H6N4O8 alloxantin 76-24-4
C8H6O benzocyclobutenone 3469-06-5
C8H6O benzofuran 271-89-6
C8H6O ethynyloxybenzene 4279-76-9
C8H6O phenyl ketene 3496-32-0
C8H6O2 isophthalaldehyde 626-19-7
C8H6O2 phenylglyoxal 1074-12-0
C8H6O3 benzoylformic acid 611-73-4
C8H6O3 piperonal 120-57-0
C8H7Br bromocubane 59346-69-9
C8H7ClO benzeneacetyl chloride 103-80-0
C8H7ClO2 benzyl chloroformate 501-53-1
C8H7F2NO difluoroacetanilide 404-17-1
C8H7F7O3 ethyl heptafluorobutanoylacetate 336-62-9
C8H7I iodocubane 74725-77-2
C8H7N benzeneacetonitrile 140-29-4
C8H7N indole 120-72-9
C8H7N indolizine 274-40-8
C8H7NO benzyl isocyanate 3173-56-6
C8H7NO3 oxanilic acid 500-72-1
C8H7NO3 phthaldehydic acid oxime 6383-59-1
C8H7NS thiocyanic acid benzyl ester 3012-37-1
C8H7N3O5 furazolidone 67-45-8
C8H8 cubane 277-10-1
C8H8 heptafulvene 539-79-7
C8H8 styrene 100-42-5
C8H8 cyclooctatetraene 629-20-9
C8H8BrCl2O3PS bromophos 2104-96-3
C8H8Cl2IO3PS iodofenphos 18181-70-9
C8H8Cl3O3PS O,O-Dimethyl O-(2,4,5-trichlorophenyl) phosphorothioate 299-84-3
C8H8Cl3N3O4S2 trichlormethiazide 133-67-5
C8H8F5NSi aminodimethylpentafluorophenylsilane 55804-98-3
C8H8HgO2 phenyl mercurie acetate 62-38-4
C8H8N2O2 isonitrosoacetanilide 1769-41-1
C8H8N2O2 isophthalamide 1740-57-4
C8H8N2O2 terephthalamide 3010-82-0
C8H8N4 hydralazine 86-54-4
C8H8N6O6 ammonium purpurate 3051-09-0
C8H8O acetophenone 98-86-2
C8H8O benzeneacetaldehyde 122-78-1
C8H8O phthalan 496-14-0
C8H8O vinylphenyl ether 766-94-9
C8H8O2 benzeneacetic acid 103-82-2
C8H8O3 hydroxytoluic acid 83-40-9
C8H8O3 resorcinol monoacetate 102-29-4
C8H8O3 vanillin 121-33-5
C8H8O3o-vanillin 148-53-8
C8H8O4 vanillic acid 121-34-6
C8H8O4 dehydroacetic acid 520-45-6
C8H8S2 benzodithiene 6247-55-8
C8H8S4 dimethyltetrathiafulvalene 62024-60-6
C8H9ClNO5PS chlorothion 500-28-7
C8H9ClO benzyl chloromethyl ether 3587-60-8
C8H9ClO chloroxylenol 88-04-0
C8H9Cl3Si phenethyltrichlorosilane 940-41-0
C8H9NO benzeneacetamide 103-81-1
C8H9NO2 acetaminophen 103-90-2
C8H9NO2 metacetamol 621-42-1
C8H9NO2 piperonylamine 2620-50-0
C8H9O3PS salithion 3811-49-2
C8H10 cyclooctatriene 29759-77-1
C8H10 dimethylbenzene 1330-20-7
C8H10 ethylbenzene 100-41-4
C8H10ClNO2 placidyl carbamate 74283-25-3
C8H10N2O4S asulam 3337-71-1
C8H10N2S ethionamide 536-33-4
C8H10N4O2 caffeine 58-08-2
C8H10N4O2 terephthalic dihydrazide 136-64-1
C8H10O benzeneethanol 60-12-8
C8H10O dimethylphenol 1300-71-6
C8H10OS ethylphenylsulfoxide 4170-80-3
C8H10O2 dicyclopropylethanedione 15940-88-2
C8H10O2 nortricyclyl formate 21892-95-5
C8H10O2 tyrosol 501-94-0
C8H10O3 methacrylic anhydride 760-93-0
C8H10O3S ethyl benzenesulfonate 515-46-8
C8H10O4 diallyl oxalate 615-99-6
C8H10O4 diethylacetylene dicarboxylate 762-21-0
C8H10O4 ethylene diacrylate 2274-11-5
C8H10Pd cyclopentadienyl allyl palladium 1271-03-0
C8H10S benzyl methyl sulfide 766-92-7
C8H10S phenylethylthiol 4410-99-5
C8H10S2 benzyl methyl disulfide 699-10-5
C8H10Se ethylselenobenzene 17774-38-8
C8H11F3O2 cyclohexyl trifluoroacetate 1549-45-7
C8H11N benzeneethanamine 64-04-0
C8H11N collidine 29611-84-5
C8H11NO metyridine 114-91-0
C8H11NO phenylethanolamine 7568-93-6
C8H11NO2 dopamine 51-61-6
C8H11NO8 iminodisuccinic acid 131669-35-7
C8H11O2P dimethyl phenylphosphonite 2946-61-4
C8H11P dimethylphenylphosphine 672-66-2
C8H12 bicyclobutylidine 6708-14-1
C8H12 cyclohexylacetylene 931-48-6
C8H12 cyclooctyne 1781-78-8
C8H12Cr2O8 tetraacetato dichromium 15020-15-2
C8H12NO5PS2 cythioate 115-93-5
C8H12N2 betahistine 5638-76-6
C8H12N2 isobutyl pyrazine 29460-92-2
C8H12N2 mebenazine 65-64-5
C8H12N2 octanedinitrile 629-40-3
C8H12N2 phenelezine 51-71-8
C8H12N2 tetramethyl butanedinitrile 3333-52-6
C8H12N2O2 pyridoxamine 85-87-0
C8H12N2O2S phenethylsulfamide 710-15-6
C8H12N2O3 barbital 57-44-3
C8H12N2O10 diethyltartrate dinitrate 13454-52-9
C8H12N6 terephthalic bisamidrazone 19173-40-1
C8H12O cyclobutyl ethynyl methyl carbinol 515-81-1
C8H12O vinyl cyclohexene monoxide 106-86-5
C8H12OS furfuryl isopropyl sulfide 1883-78-9
C8H12O2 allyl tiglate 7493-71-2
C8H12O2 dimedone 126-81-8
C8H12O2 octynoic acid 5663-96-7
C8H12O4 ethyl diacetylacetate 603-69-0
C8H12O8W2 ditungsten tetraacetate 48169-70-6
C8H13ClO cyclopentylpropionyl chloride 104-97-2
C8H13Cl3O2 hexyl trichloroacetate 37587-86-3
C8H13N cycloheptyl cyanide 32730-85-1
C8H13NO2 bemegride 64-65-3
C8H13NO2 heliotridine 520-63-8
C8H13NO2 retronecine 480-85-3
C8H13NO3 diethadione 702-54-5
C8H13NO5 diethyl formamidomalonate 6326-44-9
C8H13NS cyclohexanemethyl isothiocyanate 52395-66-1
C8H13N2O3PS thionazin 297-97-2
C8H14 cyclooctene 931-88-4
C8H14 methyl ethyl cyclopentene 19780-56-4
C8H14 methylenecycloheptane 2505-03-5
C8H14ClN5 atrazine 1912-24-9
C8H14Cl2O2 hexyl dichloroacetate 37079-04-2
C8H14Cl3O5P butonate 126-22-7
C8H14N2 cyclohexylaminoacetonitrile 1074-58-4
C8H14N2 hexamethyleneiminoacetonitrile 54714-50-0
C8H14N4OS metribuzin 21087-64-9
C8H14N4O5 glycylglycylglycylglycine 637-84-3
C8H14O cyclooctanone 502-49-8
C8H14O dimethallyl ether 628-56-8
C8H14O vinylcyclohexyl ether 2182-55-0
C8H14O2 butyl methacrylate 97-88-1
C8H14O2 cycloheptanecarboxylic acid 1460-16-8
C8H14O2 cyclohexaneacetic acid 5292-21-7
C8H14O2 cyclopentanepropanoic acid 140-77-2
C8H14O2 ethylene glycol diallyl ether 7529-27-3
C8H14O2 isopropyl tiglate 1733-25-1
C8H14O2 propyl angelate 53082-57-8
C8H14O2 propyl tiglate 61692-83-9
C8H14O2S2 lipoic acid 62-46-4
C8H14O3 carbonic acid cyclohexylmethyl ester 25066-36-8
C8H14O3 ethyl 3-oxohexanoate 3249-68-1
C8H14O4 diethyl succinate 123-25-1
C8H14O4 diisopropyl oxalate 615-81-6
C8H14O4 ethylene glycol diglycidyl ether 2224-15-9
C8H14O4 suberic acid 505-48-6
C8H14O4 sym. dimethyladipic acid 26979-55-5
C8H14O4 tetramethylbutanedioic acid 630-51-3
C8H14O5 diethyl malate 626-11-9
C8H14O6 diethyl tartrate 87-91-2
C8H14O6 triethylene glycol diformate 5451-65-0
C8H15Br cyclooctyl bromide 1556-09-8
C8H15BrO2 hexyl bromoacetate 13048-32-3
C8H15ClO octanoyl chloride 111-64-8
C8H15ClO2 hexyl chloroacetate 5927-57-1
C8H15CoNO3P triethylphosphine cobalt dicarbonyl nitrosyl 21485-16-5
C8H15N octahydroindolizine 13618-93-4
C8H15N octanenitrile 124-12-9
C8H15N tropane 529-17-9
C8H15NO hygrine 496-49-1
C8H15NO tropine 120-29-6
C8H15NO2 cyclopentanecarboxylic acid 1664-35-3
C8H15NO2 dimethylaminoethyl methacrylate 2867-47-2
C8H15NO2 ethyl pipecolinate 15862-72-3
C8H15NO2 oxanamide 126-93-2
C8H15NO2 platynecine 520-62-7
C8H15O2Tl thallium octanoate 18993-50-5
C8H16 cyclooctane 292-64-8
C8H16FO2P cyclohexyl ethylphosphonofluoridate 7284-84-6
C8H16NO3P diisopropyl cyanomethylphosphonate 21658-95-7
C8H16NO5P dicrotophos 141-66-2
C8H16N2O2S2 morpholine disulfide 103-34-4
C8H16O cycloheptanemethanol 4448-75-3
C8H16O cyclohexaneethanol 4442-79-9
C8H16O cyclooctyl alcohol 696-71-9
C8H16O diisobutylene oxide 63919-00-6
C8H16O methylheptenol 1335-09-7
C8H16O octanal 124-13-0
C8H16O2 amyl propionate 624-54-4
C8H16O2 butyl butyrate 109-21-7
C8H16O2 ethyl isocaproate 25415-67-2
C8H16O2 hexyl ethanoate 142-92-7
C8H16O2 isoamyl propionate 105-68-0
C8H16O2 isohexyl acetate 628-95-5
C8H16O2 isopropyl pivalate 5129-36-2
C8H16O2 octanoic acid 124-07-2
C8H16O2 propyl isovalerate 557-00-6
C8H16O2 valproic acid 99-66-1
C8H17ClO4 tetraethylene glycol monochlorohydrine 5197-66-0
C8H17Cl3Si octyltrichlorosilane 5283-66-9
C8H17N cycloheptanemethylamine 4448-77-5
C8H17N cyclooctanamine 5452-37-9
C8H17NO octanaloxime 929-55-5
C8H17NO octanamide 629-01-6
C8H17NO valnoctamide 4171-13-5
C8H17NO3Si ethylsilatrane 2097-16-7
C8H17NO4Si ethoxysilatrane 3463-21-6
C8H18 octane 111-65-9
C8H18AsO2 dibutylarsinic acid 2850-61-5
C8H18Cl2Si dibutyldichlorosilane 3449-28-3
C8H18FO2P heptyl methylphosphonofluoridate 162085-82-7
C8H18FO2P hexyl ethylphosphonofluoridate 135445-19-1
C8H18FO2P pinacolyl ethylphosphonofluoridate 97931-20-9
C8H18N2 diisobutyl diazene 3896-19-3
C8H18N2 isobutyraldehyde isobutylhydrazone 21041-71-4
C8H18O isobutyl ether 628-55-7
C8H18O isooctanol 26952-21-6
C8H18O isopropyl pentyl ether 5756-37-6
C8H18O pentyl propyl ether 18641-82-2
C8H18O2 hexanal dimethyl acetal 1599-47-9
C8H18O2S diisobutyl sulfone 10495-45-1
C8H18O2Si allyldiethoxymethylsilane 18388-45-9
C8H18O2Sn triethyl tin acetate 1907-13-7
C8H18O3 ethoxyacetaldehyde diethylacetal 4819-77-6
C8H18S diisobutyl sulfide 592-65-4
C8H19Al diisobutylaluminum hydride 1191-15-7
C8H19ClSi dimethylthexylsilyl chloride 67373-56-2
C8H19N ethylmethylisoamylamine 500003-01-0
C8H19N isoamylpropylamine 78579-58-5
C8H19N octodrine 543-82-8
C8H19N tertiary octyl amine 60996-53-4
C8H19NO heptaminol 372-66-7
C8H19O2PS2 ethoprophos 13194-48-4
C8H19O2PS3 disulfoton 298-04-4
C8H19O3P dibutyl hydrogen phosphite 1809-19-4
C8H19O3P diisobutylphosphite 1189-24-8
C8H19O3P methyl pinacolyl methylphosphonate 7040-59-7
C8H19O3PS3 oxydisulfoton 2497-07-6
C8H19O4PS3 disulfoton sulfone 2497-06-5
C8H20BrN tetraethylammonium bromide 71-91-0
C8H20Br4FeN tetraethylammonium tetrabromoferrate 21279-19-6
C8H20Cl4FeN tetraethylammonium tetrachloroferrate 14240-75-6
C8H20IN tetraethylammonium iodide 68-05-3
C8H20N2 tetraethylhydrazine 4267-00-9
C8H20N2OS tetraethyl sulfurous diamide 33641-61-1
C8H20N2O2S tetraethyl sulfamide 2832-49-7
C8H20O2Si diethoxydiethylsilane 5021-93-2
C8H20O3Si ethyltriethoxysilane 78-07-9
C8H20O5P2S2 sulfotep 3689-24-5
C8H20P2 tetraethyldiphosphine 3040-63-9
C8H20Pb tetraethyllead 78-00-2
C8H20Sb2 tetraethyldistibine 4669-92-5
C8H20TeZn diethylzinc diethyltellurim complex 132851-15-1
C8H23N5 tetraethylenepentamine 112-57-2
C8H24O2Si3 octamethyltrisiloxane 107-51-7
C8N6 hexacyanoethane 4383-67-9
C8(NO2)8 octanitrocubane 99393-63-2

See also


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Aliphatic compound Class of chemical compounds without aromatic ring

In organic chemistry, hydrocarbons are divided into two classes: aromatic compounds and aliphatic compounds. Aliphatic compounds can be saturated, like hexane, or unsaturated, like hexene and hexyne. Open-chain compounds, whether straight or branched, and which contain no rings of any type, are always aliphatic. Cyclic compounds can be aliphatic if they are not aromatic.

Alkene Type of chemical compound

In chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond.

Carbon Chemical element, symbol C and atomic number 6

Carbon is a chemical element with the symbol C and atomic number 6. It is nonmetallic and tetravalent—making four electrons available to form covalent chemical bonds. It belongs to group 14 of the periodic table. Carbon makes up only about 0.025 percent of Earth's crust. Three isotopes occur naturally, 12C and 13C being stable, while 14C is a radionuclide, decaying with a half-life of about 5,730 years. Carbon is one of the few elements known since antiquity.

A chemical formula is a way of presenting information about the chemical proportions of atoms that constitute a particular chemical compound or molecule, using chemical element symbols, numbers, and sometimes also other symbols, such as parentheses, dashes, brackets, commas and plus (+) and minus (−) signs. These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a chemical name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulae can fully specify the structure of only the simplest of molecules and chemical substances, and are generally more limited in power than chemical names and structural formulae.

Functional group Set of atoms in a molecule which augment its chemical and/or physical properties

In organic chemistry, a functional group is a substituent or moiety in a molecule that causes the molecule's characteristic chemical reactions. The same functional group will undergo the same or similar chemical reactions regardless of the rest of the molecule's composition. This enables systematic prediction of chemical reactions and behavior of chemical compounds and the design of chemical synthesis. The reactivity of a functional group can be modified by other functional groups nearby. Functional group interconversion can be used in retrosynthetic analysis to plan organic synthesis.

Carbon compounds are defined as chemical substances containing carbon. More compounds of carbon exist than any other chemical element except for hydrogen. Organic carbon compounds are far more numerous than inorganic carbon compounds. In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is catenation as the ability to form long carbon chains and rings.

Organic compound Chemical compound with carbon-hydrogen bonds

In chemistry, organic compounds are generally any chemical compounds that contain carbon-hydrogen bonds. Due to carbon's ability to catenate, millions of organic compounds are known. The study of the properties, reactions, and syntheses of organic compounds comprise the discipline known as organic chemistry. For historical reasons, a few classes of carbon-containing compounds, along with a few other exceptions, are not classified as organic compounds and are considered inorganic. Other than those just named, little consensus exists among chemists on precisely which carbon-containing compounds are excluded, making any rigorous definition of an organic compound elusive.

Organic chemistry Subdiscipline of chemistry, with especial focus on carbon compounds

Organic chemistry is a branch of chemistry that studies the structure, properties and reactions of organic compounds, which contain carbon-carbon covalent bonds. Study of structure determines their structural formula. Study of properties includes physical and chemical properties, and evaluation of chemical reactivity to understand their behavior. The study of organic reactions includes the chemical synthesis of natural products, drugs, and polymers, and study of individual organic molecules in the laboratory and via theoretical study.

Organometallic chemistry Study of chemical compounds containing at least one bond between a carbon atom of an organic compound and a metal

Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkaline, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and selenium, as well. Aside from bonds to organyl fragments or molecules, bonds to 'inorganic' carbon, like carbon monoxide, cyanide, or carbide, are generally considered to be organometallic as well. Some related compounds such as transition metal hydrides and metal phosphine complexes are often included in discussions of organometallic compounds, though strictly speaking, they are not necessarily organometallic. The related but distinct term "metalorganic compound" refers to metal-containing compounds lacking direct metal-carbon bonds but which contain organic ligands. Metal β-diketonates, alkoxides, dialkylamides, and metal phosphine complexes are representative members of this class. The field of organometallic chemistry combines aspects of traditional inorganic and organic chemistry.

A period 2 element is one of the chemical elements in the second row of the periodic table of the chemical elements. The periodic table is laid out in rows to illustrate recurring (periodic) trends in the chemical behavior of the elements as their atomic number increases; a new row is started when chemical behavior begins to repeat, creating columns of elements with similar properties.

Cycloalkane

In organic chemistry, the cycloalkanes are the monocyclic saturated hydrocarbons. In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring, and all of the carbon-carbon bonds are single. The larger cycloalkanes, with more than 20 carbon atoms are typically called cycloparaffins. All cycloalkanes are isomer of Alkene.

Aromaticity Phenomenon providing chemical stability in resonating hybrids of cyclic organic compounds

In chemistry, aromaticity is a property of cyclic (ring-shaped), typically planar (flat) molecular structures with pi bonds in resonance that gives increased stability compared with other geometric or connective arrangements with the same set of atoms. Aromatic rings are very stable and do not break apart easily. Organic compounds that are not aromatic are classified as aliphatic compounds—they might be cyclic, but only aromatic rings have enhanced stability.

In chemistry, an inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds, that is, a compound that is not an organic compound. However, the distinction is not clearly defined; authorities have differing views on the subject. The study of inorganic compounds is a subfield of chemistry known as inorganic chemistry.

In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry. Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be created. There is also an IUPAC nomenclature of inorganic chemistry.

Butene, also known as butylene, is an alkene with the formula C4H8. The word butene may refer to any of the individual compounds. They are colourless gases that are present in crude oil as a minor constituent in quantities that are too small for viable extraction. Butene is therefore obtained by catalytic cracking of long-chain hydrocarbons left during refining of crude oil. Cracking produces a mixture of products, and the butene is extracted from this by fractional distillation.

Bicyclic molecule Class of chemical compounds

A bicyclic molecule is a molecule that features two joined rings. Bicyclic structures occur widely, for example in many biologically important molecules like α-thujene and camphor. A bicyclic compound can be carbocyclic, or heterocyclic, like DABCO. Moreover, the two rings can both be aliphatic, or can be aromatic, or a combination of aliphatic and aromatic.

In chemical nomenclature, a preferred IUPAC name (PIN) is a unique name, assigned to a chemical substance and preferred among the possible names generated by IUPAC nomenclature. The "preferred IUPAC nomenclature" provides a set of rules for choosing between multiple possibilities in situations where it is important to decide on a unique name. It is intended for use in legal and regulatory situations.

In organic chemistry, the carbon number of a compound is the number of carbon atoms in each molecule. The properties of hydrocarbons can be correlated with the carbon number, although the carbon number alone does not give an indication of the saturation of the organic compound. When describing a particular molecule, the "carbon number" is also the ordinal position of a particular carbon atom in a chain.

This is an index of lists of molecules. Millions of molecules have existed in the universe since before the formation of Earth. Three of them, carbon dioxide, water and oxygen were necessary for the growth of life. Though we have always been surrounded by these substances, we have not always known what they were composed of.