List of compounds with carbon number 5

Last updated

This is a partial list of molecules that contain 5 carbon atoms.

Chemical formula Synonyms CAS number
C5BrMnO5 manganese pentacarbonyl bromide 14516-54-2
C5BrO5Re rhenium pentacarbonyl bromide 14220-21-4
C5Cl2F6O2 hexafluoroglutaryl chloride 678-77-3
C5F6O3 hexafluoroglutaric acid anhydride 376-68-1
C5F8O2 hexafluoroglutaryl fluoride 678-78-4
C5F10 decafluorocyclopentane 376-77-2
C5F11N undecafluoropiperidine 836-77-1
C5F13N perfluoromethyldiethylamine 758-48-5
C5FeO4S tetracarbonyl carbonothioyl iron 66517-47-3
C5FeO5 iron pentacarbonyl 13463-40-6
C5HMnO5 hydromanganese pentacarbonyl 16972-33-1
C5HN3 ethylenetricarbonitrile 997-76-2
C5H2F6O4 hexafluoroglutaric acid 376-73-8
C5H3CoF2O4Si methyldifluorosilylcobalt tetracarbonyl 26024-31-7
C5H3N3 cyanopyrazine 19847-12-2
C5H4 cyclopentadienylide radical 4729-01-5
C5H4Cl2O2 itaconyl chloride 1931-60-8
C5H4Cl6O3 clorethate 5634-37-7
C5H4F6N2O2 perfluoroglutaramide 507-68-6
C5H4N2O pyrazinecarboxaldehyde 5780-66-5
C5H4N2O2 pyrazinoic acid 98-97-5
C5H4N2O4 orotic acid 65-86-1
C5H4N4 pyridotetrazole 274-87-3
C5H4N4O allopurinol 315-30-0
C5H4N4O hypoxanthine 68-94-0
C5H4N4O2 xanthine 69-89-6
C5H4N4O3 uric acid 69-93-2
C5H4N4S tisopurine 5334-23-6
C5H4OS 2-thiophenecarboxaldehyde 98-03-3
C5H4OS 3-thiophenecarboxaldehyde 498-62-4
C5H4O3 furancarboxylic acid 26447-28-9
C5H5 cyclopentadiene 542-92-7
C5H5 cyclopentadienyl radical 2143-53-5
C5H5As arsabenzene 289-31-6
C5H5Bi bismin 289-52-1
C5H5Co cyclopentadienylcobalt 61332-89-6
C5H5F3O2 allyl trifluoroacetate 383-67-5
C5H5N pyridine 110-86-1
C5H5NOS crotonyl isothiocyanate 60034-28-8
C5H5NO2 furamide 609-38-1
C5H5NO2 mecrylate 137-05-3
C5H5N3O pyrazinamide or pyrazine carboxamide98-96-4
C5H5N5 adenine 73-24-5
C5H5Ni cyclopentadienylnickel 61332-95-4
C5H5P Phosphorine or phosphabenzene289-68-9
C5H5Sb antimonin 289-75-8
C5H6 cyclopropylacetylene 6746-94-7
C5H6BrN pyridinium bromide 18820-82-1
C5H6Cl2O2 allyl dichloroacetate 30895-77-3
C5H6Cl2O2 pentanedioyl dichloride 2873-74-7
C5H6F6NP pyridium hexafluorophosphate 16941-15-4
C5H6IN pyridium iodide 18820-83-2
C5H6N2 glutaronitrile 544-13-8
C5H6N2O2 thymine 65-71-4
C5H6O 2-methylfuran 534-22-5
C5H6O 3-methylfuran 930-27-8
C5H6O vinyl allenyl ether 4409-99-8
C5H6O2 ethyl propiolate 623-47-2
C5H6O4 citraconic acid 7407-59-2
C5H6S 2-methylthiophene 554-14-3
C5H6S 3-methylthiophene 616-44-4
C5H6S2 3-(methylthio)thiophene 20731-74-2
C5H6Si silabenzene 289-77-0
C5H7 cyclopentenyl radical 10577-65-8
C5H7ClO cyclobutanecarboxylic acid chloride 5006-22-4
C5H7ClO2 chloroacetic acid allyl ester 2916-14-5
C5H7ClO3 ethyl malonyl chloride 36239-09-5
C5H7ClO4 dimethyl chloromalonate 28868-76-0
C5H7Cl3O2 trichloroaetic acid isopropyl ester 3974-99-0
C5H7F3O2 isopropyl trifluoroacetate 400-38-4
C5H7N cyclobutanecarbonitrile 4426-11-3
C5H7N methallyl cyanide 4786-19-0
C5H7NO2 glutarimide 1121-89-7
C5H7NO3 pidolic acid 98-79-3
C5H7N3O2 dimetridazole 551-92-8
C5H8 cyclopentene 142-29-0
C5H8 ethenylcyclopropane 693-86-7
C5H8 ethylidenecyclopropane 18631-83-9
C5H8 spiropentane 157-40-4
C5H8N4O3S2 methazolamide 554-57-4
C5H8O cyclobutanecarboxaldehyde 2987-17-9
C5H8O cyclopentanone 120-92-3
C5H8O propargylethyl ether 628-33-1
C5H8O2 acetylacetone 123-54-6
C5H8O2 cyclobutane carboxylic acid 3721-95-7
C5H8O2 cyclopropaneacetic acid 5239-82-7
C5H8O2 glutaraldehyde 111-30-8
C5H8O2 angelic acid 565-63-9
C5H8O2 tiglic acid 80-59-1
C5H8O4 ethylmalonic acid 601-75-2
C5H8O4 methylene diacetate 628-51-3
C5H8O4 glutaric acid 110-94-1
C5H8S propargyl ethyl sulfide 7310-92-1
C5H9 cyclopentyl radical 3889-74-5
C5H9Br bromotrimethylethylene 3017-70-7
C5H9Cl chlorocyclopentane 930-28-9
C5H9ClO ethylmethylacetylchloride 57526-28-0
C5H9ClO pentanoyl chloride 638-29-9
C5H9ClO tetrahydrofurfuryl chloride 3003-84-7
C5H9ClO2 chloroacetic acid isopropyl ester 105-48-6
C5H9ClO2 chloroacetic acid propyl ester 5396-24-7
C5H9ClO2 isobutyl chloroformate 543-27-1
C5H9F fluorocyclopentane 1481-36-3
C5H9FO2 butyl fluoromethanoate 500023-96-1
C5H9N isobutylisocyanide 590-94-3
C5H9N pentanenitrile 110-59-8
C5H9NO piperidinone 27154-43-4
C5H9NO2 proline 147-85-3
C5H9NO2S isothiocyanatoacetaldehyde dimethyl acetal 75052-04-9
C5H9NO2S propanesulfonylacetonitrile 175137-61-8
C5H9NO3 hydroxyproline 51-35-4
C5H9NO3S acetylcysteine 616-91-1
C5H9NS isobutyl isothiocyanate 591-82-2
C5H9N3 azidocyclopentane 33670-50-7
C5H9N3 betazole 105-20-4
C5H9N3 histamine 51-45-6
C5H9O2Tl thallium pentanoate 34244-89-8
C5H10 cyclopentane 287-92-3
C5H10 ethylcyclopropane 1191-96-4
C5H10 1,1-dimethylcyclopropane 1630-94-0
C5H10 cis-1,2-dimethylcyclopropane 930-18-7
C5H10 trans-1,2-dimethylcyclopropane 2402-06-4
C5H10 methylcyclobutane 598-61-8
C5H10BrF2O3P bromodifluoromethyl diethylphosphonate 65094-22-6
C5H10ClNO4 glutamic acid hydrochloride 138-15-8
C5H10Cl2O2 pentaerythritol dichlorohydrin 2209-86-1
C5H10NO3P diethyl phosphorocyanidate 2942-58-7
C5H10N2 diethylcyanamide 617-83-4
C5H10N2O2S methomyl 16752-77-5
C5H10N2O3 alanylglycine 687-69-4
C5H10N6O4 dinitropentamethylenetetramine 949-56-4
C5H10O butenol methyl 60766-00-9
C5H10O cyclobutanemethanol 4415-82-1
C5H10O cyclopentanol 96-41-3
C5H10O cyclopropaneethanol 2566-44-1
C5H10O cyclopropyl methyl carbinol 765-42-4
C5H10O pentanal 110-62-3
C5H10O propoxyethylene 764-47-6
C5H10OS ethyl thiopropionate 2432-42-0
C5H10O2 methoxymethyl allyl ether 62322-45-6
C5H10O2 valeric acid 109-52-4
C5H10O2 pivalic acid 75-98-9
C5H10O2 sec butylformate 589-40-2
C5H10O3 hydroxy pivalic acid 4835-90-9
C5H10O3 isopropoxyacetic acid 33445-07-7
C5H10O3S ethylsulfonylpropanone 86453-13-6
C5H10O4 deoxyribose 533-67-5
C5H10O4 monoacetine 26446-35-5
C5H10O5
(aldopentoses)
arabinose 147-81-9
D-arabinose 10323-20-3
L-arabinose 87-72-9
lyxose 65-42-9
D-lyxose 1114-34-7
L-lyxose 1949-78-6
ribose
D-ribose
50-69-1
L-ribose 24259-59-4
xylose 25990-60-7
D-xylose 58-86-6
L-xylose 609-06-3
C5H10O5
(ketopentoses)
ribulose 5556-48-9
D-ribulose 488-84-6
L-ribulose
xylulose 5962-29-8
D-xylulose
L-xylulose 527-50-4
C5H10O5 1,3,5,7,9-pentaoxecane 16528-92-0
C5H10S tetrahydro-2-methylthiophene 1795-09-1
C5H10S tetrahydro-3-methylthiophene 4740-00-5
C5H10S cyclopentanethiol 1679-07-8
C5H10S trimethylthiirane 53971-47-4
C5H11 neopentyl radical 3744-21-6
C5H11Br bromopentane
C5H11BrO2Si trimethylsilyl bromoacetate 18291-80-0
C5H11ClHg isopentyl mercuric chloride 17774-08-2
C5H11ClO4 monochloropentaerythritol 36043-12-6
C5H11ClSi allylchlorodimethylsilane 4028-23-3
C5H11Cl3Si trichloropentylsilane 107-72-2
C5H11FO4 monofluoropentaerythritol 36043-13-7
C5H11N cyclopentanamine 1003-03-8
C5H11N ethyl propyliden amine 500011-12-1
C5H11N piperidine 110-89-4
C5H11N propionaldehyde ethylimine 18328-91-1
C5H11NO Several compounds
C5H11NO2 amyl nitrite 110-46-3
C5H11NO2 amyl nitrite 463-04-7
C5H11NO2 butyl carbamate 592-35-8
C5H11NO2 iso butyl carbamate 543-28-2
C5H11NO2 valine 72-18-4
C5H11NO2S methionine 59-51-8
C5H11NO2S penicillamine 52-67-5
C5H11NO4 ammonium acid pyrotartrate 61478-85-1
C5H11NS2 ethyl dithiocarbimidoic acid dimethyl ester 116072-47-0
C5H11N2O2P tabun 77-81-6
C5H11N3S piperazine hydrothiocyanate 73373-48-5
C5H11O2 pentyl peroxy radical 52310-21-1
C5H11O3P dimethyl allylphosphonate 757-54-0
C5H11O5P trimethyl phosphonoacetate 5927-18-4
C5H11P phoshorinane 4743-40-2
C5H12 pentane 109-66-0
C5H12ClO2PS2 chlormephos 24934-91-6
C5H12Cl2Si isobutylmethyldichlorosilane 18147-18-7
C5H12FO2P butyl methylphosphonofluoridate 352-63-6
C5H12FO2P isopropyl ethylphosphonofluoridate 1189-87-3
C5H12FO2P propyl ethylphosphonofluoridate 2992-95-2
C5H12NO3PS2 dimethoate 60-51-5
C5H12NO4PS omethoate 1113-02-6
C5H12N2 butylmethyldiazene 4426-46-4
C5H12N2 homopiperazine 505-66-8
C5H12N2O valeric acid hydrazide 38291-82-6
C5H12N3OP tetramethylphosphorodiamidic cyanide 14445-60-4
C5H12O isobutyl methyl ether 625-44-5
C5H12O2 diethoxymethane 462-95-3
C5H12O2Si trimethylsilyl acetate 13411-48-8
C5H12O3Si vinyltrimethoxysilane 2768-02-7
C5H12O4 tetramethoxymethane 1850-14-2
C5H12O5 adonitol 488-81-3
C5H12O5 xylitol 87-99-0
C5H13BO diethylmethoxyborane 7397-46-8
C5H13ClSi propyldimethylchlorosilane 17477-29-1
C5H13N neopentylamine 5813-64-9
C5H13NO2 methyldiethanolamine 105-59-9
C5H13NO4 monoaminopentaerythritol 36043-15-9
C5H13O2PS diethyl methylphosphonothioate 6996-81-2
C5H13O3P diethyl methanephosphonate 683-08-9
C5H13O3P isopropyl methyl methylphosphonate 690-64-2
C5H13O4P diethyl hydroxymethylphosphonate 3084-40-0
C5H14Cl2N2O2 ornithine dihydrochloride 6211-16-1
C5H14NO6P betaine phosphate 58823-88-4
C5H14N2 ethyl trimethylhydrazine 50599-41-2
C5H14N2O4 diaminopentaerythritol 36043-16-0
C5H14O2Si methyldiethoxysilane 2031-62-1
C5H14O3Si trimethoxyethylsilane 5314-55-6
C5H14O6P2 tetramethyl methylenediphosphonate 16001-93-7
C5H15As5 pentamethylpentaarsolane 20550-47-4
C5H15N2OP pentamethylphosphonic diamide 2511-17-3
C5H15Sb pentamethylantimony 15120-50-0
C5H15Ta pentamethyl tantalum 53378-72-6
C5H16Cl4MnN2 pentyldiamine manganese tetrachloride 59890-70-9
C5H30Bi2Br11N5 methylammonium bismuth bromide 119931-90-7
C5N4 methanetetracarbonitrile 24331-09-7

See also


Related Research Articles

<span class="mw-page-title-main">Alkane</span> Type of saturated hydrocarbon compound

In organic chemistry, an alkane, or paraffin, is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. Alkanes have the general chemical formula CnH2n+2. The alkanes range in complexity from the simplest case of methane, where n = 1, to arbitrarily large and complex molecules, like pentacontane or 6-ethyl-2-methyl-5-(1-methylethyl) octane, an isomer of tetradecane.

<span class="mw-page-title-main">Aliphatic compound</span> Hydrocarbon compounds without aromatic rings

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.

<span class="mw-page-title-main">Alkene</span> Hydrocarbon compound containing one or more C=C bonds

In organic chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond. The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins.

<span class="mw-page-title-main">Carbon</span> Chemical element, symbol C and atomic number 6

Carbon is a chemical element; it has symbol C and atomic number 6. It is nonmetallic and tetravalent—meaning that its atoms are able to form up to four covalent bonds due to its valence shell exhibiting 4 electrons. It belongs to group 14 of the periodic table. Carbon makes up 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.

In chemistry, 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 since it does not contain any 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.

<span class="mw-page-title-main">Functional group</span> 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.

<span class="mw-page-title-main">Organic compound</span> Chemical compound with carbon-hydrogen bonds

In chemistry, many authors consider an organic compound to be any chemical compound that contains carbon–hydrogen or carbon–carbon bonds; however, some authors consider an organic compound to be any chemical compound that contains carbon. The definition of "organic" versus "inorganic", and whether some other carbon-containing compounds are organic or inorganic vary from author to author, and are topics of debate. For example, carbon-containing compounds such as alkanes and its derivatives are considered organic, but many others are considered inorganic, such as halides of carbon without carbon-hydrogen and carbon-carbon bonds, and certain compounds of carbon with nitrogen and oxygen.

<span class="mw-page-title-main">Organic chemistry</span> Subdiscipline of chemistry, focusing on carbon compounds

Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. 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.

<span class="mw-page-title-main">Organometallic chemistry</span> Study of organic compounds containing metal(s)

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 alkali, 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.

<span class="mw-page-title-main">Cycloalkane</span> Saturated alicyclic hydrocarbon

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 isomers of alkenes.

<span class="mw-page-title-main">Aromaticity</span>

In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone. The earliest use of the term was in an article by August Wilhelm Hofmann in 1855. There is no general relationship between aromaticity as a chemical property and the olfactory properties of such compounds.

In chemistry, an inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds⁠that is, a compound that is not an organic compound. 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.

In chemistry, halogenation is a chemical reaction that entails the introduction of one or more halogens into a compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. This kind of conversion is in fact so common that a comprehensive overview is challenging. This article mainly deals with halogenation using elemental halogens. Halides are also commonly introduced using salts of the halides and halogen acids. Many specialized reagents exist for and introducing halogens into diverse substrates, e.g. thionyl chloride.

<span class="mw-page-title-main">Bicyclic molecule</span> Molecule with two joined rings

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.

<span class="mw-page-title-main">Cyclic compound</span> Molecule with a ring of bonded atoms

A cyclic compound is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring. Rings may vary in size from three to many atoms, and include examples where all the atoms are carbon, none of the atoms are carbon, or where both carbon and non-carbon atoms are present. Depending on the ring size, the bond order of the individual links between ring atoms, and their arrangements within the rings, carbocyclic and heterocyclic compounds may be aromatic or non-aromatic; in the latter case, they may vary from being fully saturated to having varying numbers of multiple bonds between the ring atoms. Because of the tremendous diversity allowed, in combination, by the valences of common atoms and their ability to form rings, the number of possible cyclic structures, even of small size numbers in the many billions.

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. Although humanity had always been surrounded by these substances, it has not always known what they were composed of.