List of compounds with carbon number 2

Last updated

This is a partial list of molecules that contain 2 carbon atoms.

Chemical formulaSynonymsCAS number
C2Al monoaluminum dicarbide 37297-57-7
C2Al2 dialuminum dicarbide 12122-01-9
C2B boron dicarbide 12539-98-9
C2Be beryllium dicarbide 12070-28-9
C2BrCl bromochloroacetylene 25604-70-0
C2BrClF2O bromodifluoroacetylchloride 3832-48-2
C2BrCl5 bromopentachloroethane 79504-02-2
C2BrF5 bromopentafluoroethane 354-55-2
C2Br2FN dibromo fluoroacetonitrile 6698-74-4
C2Br2N2O2 dibromofuroxan 70134-71-3
C2Br2O2 oxalyl bromide 15219-34-8
C2Br6 hexabromoethane 594-73-0
C2Ca calcium carbide 75-20-7
C2Ce cerium dicarbide 12012-32-7
C2CeRh cerium rhodium dicarbide 53262-56-9
C2Cl2F2 dichlorodifluoroethylene 27156-03-2
C2Cl2O2 oxalyl chloride 79-37-8
C2Cl3N trichloroacetonitrile 108-77-0
C2Cl4 tetrachloroethylene 127-18-4
C2Cl4O trichloroacetyl chloride 76-02-8
C2Cl4O2 trichloromethyl chloroformate 503-38-8
C2Cl5F pentachlorofluoroethane 354-56-3
C2CoNO3 cobalt dicarbonyl nitrosyl 61332-94-3
C2Dy dysprosium dicarbide 12175-80-3
C2Er erbium dicarbide 12192-37-9
C2Eu europium dicarbide 12127-44-5
C2FN5O10 fluoropentanitroethane 23072-51-7
C2F2O2 oxalyl fluoride 359-40-0
C2F3 trifluorovinyl radical 4605-17-8
C2F3I iodotrifluoroethylene 359-37-5
C2F3N trifluoromethylisocyanide 105879-13-8
C2F5 pentafluoro ethyl radical 3369-48-0
C2F5I pentafluoroethyliodide 354-64-3
C2F6O5S2 trifluoromethanesulfonic anhydride 358-23-6
C2F7N perfluoroethanamine 354-80-3
C2H ethynyl radical 2122-48-7
C2HBrClF3 halothane 151-67-7
C2HBrO bromoketene 78957-22-9
C2HBr2FO2 dibromofluoroacetic acid 353-99-1
C2HBr3 tribromoethene 598-16-3
C2HBr3O2 tribromoacetic acid 75-96-7
C2HClO chloroketene 29804-89-5
C2HCl3 trichloroethylene 79-01-6
C2HCl3O chloral 75-87-6
C2HF3OS trifluorothiolacetic acid 2925-25-9
C2HF5O pentafluorodimethyl ether 3822-68-2
C2HNO formyl cyanide 4471-47-0
C2HO ethynyloxy radical 51095-15-9
C2H2 acetylene 74-86-2
C2H2AsCl3 lewisite 541-25-3
C2H2BrClO bromoacetyl chloride 22118-09-8
C2H2Br2O bromoacetyl bromide 598-21-0
C2H2Br2O2 dibromoethanoic acid 631-64-1
C2H2Cl2 dichloromethane
C2H2ClF2NO chlorodifluoroacetamide 354-28-9
C2H2ClNS chloromethyl thiocyanate 3268-79-9
C2H2Cl2O dichloroacetaldehyde 79-02-7
C2H2FN fluoroacetonitrile 503-20-8
C2H2F2O2 difluoroacetic acid 381-73-7
C2H2IN iodoacetonitrile 624-75-9
C2H2N cyanomethyl radical 2932-82-3
C2H2O ethynol 32038-79-2
C2H2O ketene 463-51-4
C2H2O oxirene 157-18-6
C2H2OS ethynesulfenic acid 121564-25-8
C2H2O2 glyoxal 107-22-2
C2H2O3 formic acid anhydride 1558-67-4
C2H2O4 oxalic acid 144-62-7
C2H2O8Pb3 basic lead carbonate 1319-46-6
C2H2S thioketene 18282-77-4
C2H2Se selenoketene 61134-37-0
C2H3 vinyl radical 2669-89-8
C2H3BF2 vinyldifluoroborane 358-95-2
C2H3BrO acetyl bromide 506-96-7
C2H3Br3O2 bromal hydrate 507-42-6
C2H3Cl methylchlorocarbene 31304-51-5
C2H3ClO acetyl chloride 75-36-5
C2H3ClO2S methoxycarbonylsulfenyl chloride 26555-40-8
C2H3Cl3O2 chloral hydrate 302-17-0
C2H3FO acetyl fluoride 557-99-3
C2H3F2NO difluoroacetamide 359-38-6
C2H3F3O2Si silyl trifluoroacetate 6876-44-4
C2H3F3S2 methyl trifluoromethyl disulfide 14410-21-0
C2H3IO acetyl iodide 507-02-8
C2H3KO2 potassium acetate 127-08-2
C2H3N acetonitrile 75-05-8
C2H3NO methylcyanate 1768-34-9
C2H3NO nitrosoethylene 54680-52-3
C2H3NO2 nitroethene 500016-67-1
C2H3NO2 nitroethylene 3638-64-0
C2H3NO3 oxamic acid 471-47-6
C2H3NO4 acetyl nitrate 591-09-3
C2H3NSe methyl isoselenocyanate 4426-70-4
C2H3NSe methyl selenocyanate 2179-80-8
C2H3NaO2 sodium ethanoate 127-09-3
C2H3O acetyl radical 3170-69-2
C2H3O oxiranyl radical 31586-84-2
C2H3O vinyloxy radical 6912-06-7
C2H3O2Tl thallium acetate 563-68-8
C2H4 ethylene 74-85-1
C2H4ClO2P ethylene chlorophosphite 822-39-9
C2H4Cl2 dichloroethane 1300-21-6
C2H4F2O difluoroethanol 359-13-7
C2H4N2O2 oxalamide 471-46-5
C2H4N2O4 dihydroxyglyoxime 1687-60-1
C2H4N2S2 ethanedithioamide 79-40-3
C2H4N4 dicyanodiamide 461-58-5
C2H4N4O2 diazenedicarboxamide 123-77-3
C2H4O acetaldehyde 75-07-0
C2H4O ethenol 557-75-5
C2H4O ethylene oxide 75-21-8
C2H4OS ethanethioic acid 507-09-5
C2H4OS ethenesulfenic acid 2492-74-2
C2H4O2 acetic acid 64-19-7
C2H4O2 1,2-dioxetane 6788-84-7
C2H4O2 formaldehyde dimer 61233-19-0
C2H4O2 methyl formate 107-31-3
C2H4O2 glycolaldehyde 141-46-8
C2H4O3 ethaneperoxoic acid 79-21-0
C2H4O3 monomethyl carbonate 7456-87-3
C2H4O4 formic acid dimer 14523-98-9
C2H4S thiirane 420-12-2
C2H4S thioacetaldehyde 6851-93-0
C2H4Se selenoacetaldehyde 67281-48-5
C2H4Se3 triselenothane 121400-83-7
C2H5 ethyl radical 2025-56-1
C2H5BCl2 ethyldichloroborane 1739-53-3
C2H5BF2 ethylidifluoroborane 430-41-1
C2H5BrHg ethylmercuric bromide 107-26-6
C2H6Hg dimethylmercury 593-74-8
C2H5BrO bromomethyl methyl ether 13057-17-5
C2H5Cl ethyl chloride 75-00-3
C2H5ClN2O chloroacetyl hydrazine 30956-28-6
C2H5ClO ethyl hypochlorite 624-85-1
C2H5ClO2S ethanesulfonyl chloride 594-44-5
C2H5ClS chloromethylmethyl sulfide 2373-51-5
C2H5Cl2O2P ethyl dichlorophosphate 1498-51-7
C2H5Cl2P ethyldichlorophosphine 1498-40-4
C2H5Cl2PSe ethylphosphonoselenoic dichloride 14705-46-5
C2H5Cl3Si ethyltrichlorosilane 115-21-9
C2H5FO methoxymethyl fluoride 460-22-0
C2H5FO2S ethane sulfonyl fluoride 754-03-0
C2H5HgI ethylmercuric iodide 2440-42-8
C2H5I iodoethane 75-03-6
C2H5IO iodomethyl methyl ether 13057-19-7
C2H5IS iodomethyl methyl sulfide 43034-68-0
C2H5Li ethyl lithium 811-49-4
C2H5N acetaldimine 20729-41-3
C2H5N ethenamine 593-67-9
C2H5N ethylenimine 151-56-4
C2H5NO acetaldoxime 107-29-9
C2H5NO acetamide 60-35-5
C2H5NO nitrosoethane 925-91-7
C2H5NOS aminothioacetic acid 758-10-1
C2H5NO2 glycine 56-40-6
C2H5NO2 glycolamide 598-42-5
C2H5NO2S vinylsulfonamide 2386-58-5
C2H5NO4 ammonium acid oxalate 5972-72-5
C2H5NS ethanethioamide 62-55-5
C2H5N3O2 imidodicarbonic diamide 108-19-0
C2H5O ethoxy radical 2154-50-9
C2H5P phosphirane 6569-82-0
C2H5P vinyl phosphine 58436-39-8
C2H5PS2 phosphenodithioic ethane 41391-49-5
C2H5S methylthiomethyl radical 31533-72-9
C2H6 ethane 74-84-0
C2H6AlCl dimethylaluminum chloride 1184-58-3
C2H6AsBr dimethylarsine bromide 676-71-1
C2H6AsCl chlorodimethylarsine 557-89-1
C2H6BBr dimethylboron bromide 5158-50-9
C2H6BCl chlorodimethylborane 1803-36-7
C2H6BClFN dimethylaminofluorochloroborane 38481-07-1
C2H6BClO2 chlorodimethoxyborane 868-81-5
C2H6BFO2 fluorodimethoxyborane 367-46-4
C2H6Be dimethylberyllium 506-63-8
C2H6ClOP dimethylphosphinic chloride 1111-92-8
C2H6ClO2P dimethylchlorophosphite 3743-07-5
C2H6ClPS dimethylphosphinothioic chloride 993-12-4
C2H6Cl2Ge dimethylgermanium dichloride 1529-48-2
C2H6Cl2Si ethyldichlorosilane 1789-58-8
C2H6FO2P methyl methylphosphonofluoridate 353-88-8
C2H6FP dimethyl fluorophosphine 507-15-3
C2H6F3NS dimethylaminosulfur trifluoride 3880-03-3
C2H6GeO dimethylgermanone 5061-27-8
C2H6GeS dimethylgermathione 16090-49-6
C2H6N dimethyl amidogen 15337-44-7
C2H6N2O2 ethylnitramine 19091-98-6
C2H6N2O4 hydrazinium hydrogen oxalate 20321-02-2
C2H6O dimethyl ether 115-10-6
C2H6O ethanol 64-17-5
C2H6OS dimethyl sulfoxide 67-68-5
C2H6OS2 methyl methanethiosulfinate 13882-12-7
C2H6O2 ethyl hydroperoxide 3031-74-1
C2H6O2 ethylene glycol 107-21-1
C2H6O2S dimethyl sulfone 67-71-0
C2H6O2S2 methyl methanethiosulfonate 2949-92-0
C2H6O4 dioxybismethanol 17088-73-2
C2H6O5S2 methanesulfonic anhydride 7143-01-3
C2H6S dimethyl sulfide 75-18-3
C2H6S ethanethiol 75-08-1
C2H6S5 dimethyl pentasulfide 7330-31-6
C2H6Se dimethyl selenide 593-79-3
C2H6Se2 dimethyl diselenide 7101-31-7
C2H6Si2 disilyl acetylene 1070-76-4
C2H6Sn dimethylstannylene radical 23120-99-2
C2H6Te dimethyltelluride 593-80-6
C2H6Zn dimethylzinc 544-97-8
C2H7As dimethylarsine 593-57-7
C2H7AsO3 ethylarsonic acid 507-32-4
C2H7BF3N dimethylaminetrifluoroborane 811-59-6
C2H7BO2 ethyldihydroxyborane 4433-63-0
C2H7ClO dimethyl ether hydrogen chloride complex 24521-77-5
C2H7N ethylamine 75-04-7
C2H7NO acetaldehyde ammonia trimer 75-39-8
C2H7NO ethanolamine 141-43-5
C2H7NO2S ethanesulfonamide 1520-70-3
C2H7NO3S taurine 91105-79-2
C2H7NO4S2 dimethane sulfonamide 5347-82-0
C2H7NS mercaptamine 60-23-1
C2H7O3P ethylphosphonic acid 15845-66-6
C2H8BF4N dimethylammonium tetrafluoroborate 16970-97-1
C2H8BrN ethylammoniumbromide 593-55-5
C2H8N2 ethylenediamine 107-15-3
C2H8N2O4 ammonium oxalate 1113-38-8
C2H8O2Si dimethoxysilane 5314-52-3
C2H9N2O3 ethylammonium nitrate 22113-86-6
C2H10N2O8S2Fe ferrous ethylenediammonium sulfate 63589-59-3
C2H12CdTe dimethylcadmium·dimethyltellurium 143481-66-7
C2H12N6O4S guanidine sulfate 594-14-9
C2HgN2S2 mercuric thiocyanate 592-85-8
C2Ho holmium dicarbide 12071-14-6
C2K2N2 potassium cyanide dimer 55186-08-8
C2La lanthanum dicarbide 12071-15-7
C2Li2 lithium carbide 1070-75-3
C2Lu lutetium dicarbide 12175-89-2
C2Mg magnesium carbide 12122-46-2
C2N2 bisisocyanide 78800-21-2
C2N2 cyanogen 460-19-5
C2N2Na2 sodium cyanide 55186-09-9
C2N2O cyanogen isocyanate 22430-66-6
C2N2S cyanogen isothiocyanate 56023-03-1
C2N2S sulfur dicyanide 627-52-1
C2N2S2 thiocyanogen 505-14-6
C2N2Se selenium cyanide 2180-01-0
C2N4O6 trinitroacetonitrile 630-72-8
C2N6O12 hexanitroethane 918-37-6
C2Na2 Sodium carbide 2881-62-1
C2Na2O4 sodium oxalate 62-76-0
C2Nd neodymium dicarbide 12071-21-5
C2O dicarbon monoxide 12071-23-7
C2P dicarbon phosphide 12602-39-0
C2Rh rhodium dicarbide 37306-47-1
C2Sc scandium dicarbide 12175-91-6
C2Si silicon dicarbide 12071-27-1
C2Si2 disiladicarbide 12144-09-1
C2Th thorium dicarbide 12071-31-7
C2Ti titanium dicarbide 12071-32-8
C2U uranium dicarbide 12071-33-9
C2V vanadium dicarbide 12542-39-1
C2Y yttrium dicarbide 12071-35-1
C2Zr zirconium dicarbide 12340-54-4

See also


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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.

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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.