List of compounds with carbon number 3

Last updated

This is a partial list of molecules that contain 3 carbon atoms.

Chemical formulaSynonyms CAS number
C3Al4 aluminium carbide 1299-86-1
C3BrF7 heptafluoropropyl bromide 422-85-5
C3BrN bromocyanoacetylene 3114-46-3
C3ClF5O chloropentafluoroacetone 79-53-8
C3ClF5O pentafluoropropionyl chloride 422-59-3
C3ClN chlorocyanoacetylene 2003-31-8
C3Cl3NO2 trichloroacetyl isocyanate 3019-71-4
C3Cl3N3 cyanuric chloride 108-77-0
C3Cl3N3O3 trichloroisocyanuric acid 87-90-1
C3Cl5FO fluoropentachloroacetone 2378-08-7
C3Cl6 hexachlorocyclopropane 2065-35-2
C3CoNO4 cobalt tricarbonyl nitrosyl 14096-82-3
C3Cr7 chromium carbide 12075-40-0
C3F4 perfluoroallene 461-68-7
C3F6O pentafluoropropionyl fluoride 422-61-7
C3HCl2N3O3 dichloroisocyanuric acid 2782-57-2
C3HCl3O2 trichloroacrylic acid 2257-35-4
C3HF5O2 pentafluoropropionic acid 422-64-0
C3HF6N hexafluoroacetone imine 1645-75-6
C3HN isocyanoacetylene 66723-45-3
C3HN propiolonitrile 1070-71-9
C3HNO cyanoketene 4452-08-8
C3H2 cyclopropenylidene 16165-40-5
C3H2 propadienylidene 60731-10-4
C3H2ClF5O enflurane 13838-16-9
C3H2ClNO2 chloroacetyl isocyanate 4461-30-7
C3H2Cl2O2 malonyl dichloride 1663-67-8
C3H2F5NO pentafluoropropionamide 354-76-7
C3H2N2 malononitrile 109-77-3
C3H2O propadienal 61244-93-7
C3H2O2 propiolic acid 471-25-0
C3H3 cyclopropenyl radical 28933-84-8
C3H3 propargyl radical 2932-78-7
C3H3Br3O2 methyl tribromoacetate 3222-05-7
C3H3ClO3 methyl oxalyl chloride 5781-53-3
C3H3F3N2O2 trifluoroacetylurea 760-41-8
C3H3F5O methyl pentafluoroethyl ether 22410-44-2
C3H3NO acetyl cyanide 631-57-2
C3H3NO isoxazole 288-14-2
C3H3NO oxazole 288-42-6
C3H3NO propiolamide 7341-96-0
C3H3NS isothiazole 288-16-4
C3H3NS thiazole 288-47-1
C3H3O propenoyl radical 72241-20-4
C3H4 cyclopropene 2781-85-3
C3H4 propyne 74-99-7
C3H4BrClO2 methyl bromochloroacetate 20428-74-4
C3H4Cl2F2O methoxyflurane 76-38-0
C3H4F2O2 methyl difluoroacetate 433-53-4
C3H4N2 methyleneaminoacetonitrile 109-82-0
C3H4O cyclopropanone 5009-27-8
C3H4O methoxyacetylene 6443-91-0
C3H4O methylketene 6004-44-0
C3H4O2 glycidaldehyde 765-34-4
C3H4O2 propanedial 542-78-9
C3H4O3 ethylene carbonate 96-49-1
C3H4O3 methyl glyoxylate 922-68-9
C3H4O3 pyruvic acid 127-17-3
C3H4O3 tartronaldehyde 497-15-4
C3H4O4 malonic acid 141-82-2
C3H4O5 tartronic acid 80-69-3
C3H4S methylthioacetylene 10152-75-7
C3H4S thioacrolein 53439-64-8
C3H5 allyl radical 1981-80-2
C3H5 cyclopropyl radical 2417-82-5
C3H5Br cyclopropyl bromide 4333-56-6
C3H5BrO propionyl bromide 598-22-1
C3H5ClN2 imidazole hydrochloride 1467-16-9
C3H5ClO epichlorohydrin 13403-37-7
C3H5ClO propanoyl chloride 79-03-8
C3H5ClO2 chloromethyl ethanoate 625-56-9
C3H5ClO2 methoxyacetyl chloride 38870-89-2
C3H5Cl2OP allylphosphonic dichloride 1498-47-1
C3H5CsO2 caesium propionate 38869-24-8
C3H5FO propionyl fluoride 430-71-7
C3H5FO2 methyl fluoroacetate 453-18-9
C3H5KO2 potassium propionate 327-62-8
C3H5LiO2 lithium propionate 6531-45-9
C3H5N cyclopropanimine 54376-32-8
C3H5N propanenitrile 107-12-0
C3H5N propargylamine 2450-71-7
C3H5N vinylimine 18295-52-8
C3H5NO acrylamide 79-06-1
C3H5NO methoxyacetonitrile 1738-36-9
C3H5NOS methoxymethyl isothiocyanate 19900-84-6
C3H5NO2S methanesulfonylacetonitrile 2274-42-2
C3H5NO3 nitroacetone 10230-68-9
C3H5N3O3 glyoxylic acid semicarbazone 928-73-4
C3H5N3O9 nitroglycerin 55-63-0
C3H5NaO2 sodium propanoate 137-40-6
C3H5O propionyl radical 15843-24-0
C3H5O2Rb rubidium propionate 19559-54-7
C3H5O2Tl thallium propionate 63424-48-6
C3H6 cyclopropane 75-19-4
C3H6 propene 115-07-1
C3H6BrNO4 bronopol 52-51-7
C3H6Cl2Si dichloromethylvinylsilane 124-70-9
C3H6N2O2 cycloserine 68-41-7
C3H6N2O2 propanediamide 108-13-4
C3H6N2S ethenylthiourea 1483-58-5
C3H6O acetone 67-64-1
C3H6O cyclopropanol 16545-68-9
C3H6O oxetane 503-30-0
C3H6O propanal 123-38-6
C3H6O propylene oxide 75-56-9
C3H6OS ethyl thioformate 21071-39-6
C3H6OSe methylselenoacetate 209530-82-5
C3H6O2 glycidol 556-52-5
C3H6O2 propanoic acid 79-09-4
C3H6O2 Hydroxyacetone 116-09-6
C3H6O3 lactic acid 598-82-3
C3H6O3 methoxymethyl formate 4382-75-6
C3H6O3 methylene glycol monoacetate 86011-33-8
C3H6O3 methylglyoxal hydrate 1186-47-6
C3H6S allyl mercaptan 870-23-5
C3H6S methyl vinyl sulfide 1822-74-8
C3H6S thietane 287-27-4
C3H6S thioacetone 4756-05-2
C3H6S2 methyl dithioacetate 2168-84-5
C3H7 isopropyl radical 2025-55-0
C3H7BF2 isopropyldifluoroborane 3857-03-2
C3H7BrHg isopropryl mercuric bromide 18819-83-5
C3H7ClHg chloropropylmercury 2440-40-6
C3H7ClHg isopropyl mercuric chloride 30615-19-1
C3H7ClN6 melamine hydrochloride 626-32-4
C3H7Cl2P dichloropropylphosphine 15573-31-6
C3H7Cl3Si dichloromethylmethyldichlorosilane 18171-56-7
C3H7HgI isopropyl mercuric iodide 38455-14-0
C3H7N azetidine 503-29-7
C3H7N cyclopropylamine 765-30-0
C3H7NO isoxazolidine 504-72-3
C3H7NO propanamide 79-05-0
C3H7NO2 alanine 56-41-7
C3H7NO2 nitropropane 25322-01-4
C3H7NO2 propyl nitrite 543-67-9
C3H7NO2 sarcosine 107-97-1
C3H7NO2 urethane 51-79-6
C3H7NO3 isoserine 632-12-2
C3H7S propylthio radical 4985-58-4
C3H8 propane 74-98-6
C3H8Cl2Si dichloroethylmethylsilane 4525-44-4
C3H8FO2P ethyl methylphosphonofluoridate 673-97-2
C3H8FO2P methyl ethylphosphonofluoridate 665-03-2
C3H8N2 pyrazolidine 504-70-1
C3H8N2O3 dimethanolurea 140-95-4
C3H8N4O2 propanedioyl dihydrazide 3815-86-9
C3H8O isopropyl alcohol 67-63-0
C3H8OS2 dimercaprol 59-52-9
C3H8O2 propylene glycol 57-55-6
C3H8O2 propylhydroperoxide 6068-96-8
C3H8O2S ethanesulfinic acid methyl ester 31401-21-5
C3H8O2S monothioglycerol 96-27-5
C3H8O3S sulfurous acid ethyl methyl ester 10315-59-0
C3H8S2 2,4-dithiapentane 1618-26-4
C3H8S2 methyl ethyl disulfide 20333-39-5
C3H8Si silacyclobutane 287-29-6
C3H9Al trimethylaluminium 75-24-1
C3H9AsS dimethyl methylthioarsine 38859-90-4
C3H9AsSe dimethyl methylselenoarsine 73076-88-7
C3H9BF3N trimethylaminetrifluoroborane 420-20-2
C3H9BS3 trimethyl trithioborate 997-49-9
C3H9BrGe bromotrimethylgermane 1066-37-1
C3H9BrPb trimethyl lead bromide 6148-48-7
C3H9BrSi bromotrimethylsilane 2857-97-8
C3H9BrSn trimethyltin bromide 1066-44-0
C3H9Br2Sb trimethylantimony dibromide 24606-08-4
C3H9ClFSb chlorofluorotrimethylantimony 13077-54-8
C3H9ClGe trimethylgermanium chloride 1529-47-1
C3H9ClPb trimethyllead chloride 1520-78-1
C3H9Cl2Sb trimethylantimony dichloride 13059-67-1
C3H9FGe trimethylgermyl fluoride 661-37-0
C3H9Ga gallium trimethyl 1445-79-0
C3H9ISi iodotrimethylsilane 16029-98-4
C3H9I2Sb trimethylantimony diiodide 13077-53-7
C3H9In trimethylindium 3385-78-2
C3H9N ethylmethylamine 624-78-2
C3H9N isopropylamine 75-31-0
C3H9N propylamine 107-10-8
C3H9N trimethylamine 75-50-3
C3H9NO N-Methylethanolamine 109-83-1
C3H9NO dimethylaminomethanol 14002-21-2
C3H9NO trimethylhydroxylamine 5669-39-6
C3H9N3OS cysteine hydrazide 70470-68-7
C3H9N3Si azidotrimethylsilane 4648-54-8
C3H9N9 cyanuric trihydrazide 10105-42-7
C3H9OP trimethylphosphine oxide 676-96-0
C3H9PS dimethyl methylthiophosphine 35449-60-6
C3H9PS trimethylphosphine sulfide 2404-55-9
C3H9PSe dimethyl methylselenophosphine 24490-39-9
C3H9P2 trimethyldiphosphinyl radical 89148-95-8
C3H9Si trimethylsilyl radical 16571-41-8
C3H9Sn trimethyltin 17272-57-0
C3H9Tl trimethyl thallium 3003-15-4
C3H10CdCl3N trimethylammonium trichlorocadmate 68778-49-4
C3H10Ge trimethylgermane 1449-63-4
C3H10N2 1,3-Diaminopropane 109-76-2
C3H10N2O3 isopropylamine nitrate 87478-71-5
C3H10O3Si trimethoxysilane 2487-90-3
C3H10Si isopropylsilane 18230-84-7
C3H12CdCl4N2 propyldiammonium cadmium tetrachloride 60970-45-8
C3H12Cl4MnN2 propyldiammonium manganese tetrachloride 59683-18-0
C3H12N6O3 guanidine carbonate 593-85-1
C3IN iodocyanoacetylene 2003-32-9
C3La lanthanum tricarbide 12602-63-0
C3Mg2 magnesium carbide 12151-74-5
C3N cyanoethynyl radical 12543-75-8
C3N2O oxopropanedinitrile 1115-12-4
C3N3P tricyanophosphine 1116-01-4
C3O2 carbon suboxide 504-64-3
C3Si2 disilicon tricarbide 12327-32-1
C3Th thorium tricarbide 69553-67-9

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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.

In chemistry, an element is a pure substance consisting only of atoms that all have the same numbers of protons in their nuclei. Unlike chemical compounds, chemical elements cannot be broken down into simpler substances by any chemical reaction. The number of protons in the nucleus is the defining property of an element, and is referred to as its atomic number – all atoms with the same atomic number are atoms of the same element. All of the baryonic matter of the universe is composed of chemical elements. When different elements undergo chemical reactions, atoms are rearranged into new compounds held together by chemical bonds. Only a minority of elements, such as silver and gold, are found uncombined as relatively pure native element minerals. Nearly all other naturally occurring elements occur in the Earth as compounds or mixtures. Air is primarily a mixture of the elements nitrogen, oxygen, and argon, though it does contain compounds including carbon dioxide and water.

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.