List of compounds with carbon number 15

Last updated

This is a partial list of molecules that contain 15 carbon atoms.

Chemical formulaSynonymsCAS number
C15F33N perfluorotripentylamine 338-84-1
C15H8O5 Coumestrol 479-13-0
C15H8O6 Rhein 478-43-3
C15H10BrClN4S brotizolam 57801-81-7
C15H10ClFN2O desalkylflurazepam 2886-65-9
C15H10ClN3O3 clonazepam 1622-61-3
C15H10Cl2N2O delorazepam 2894-67-9
C15H10Cl2N2O2 lorazepam 846-49-1
C15H10CrO3 biphenylchromium tricarbonyl 12111-60-3
C15H10FN3O3 desmethylflunitrazepam 2558-30-7
C15H10N2O2 methylene diphenyl diisocyanate 26447-40-5
C15H10O2 benzalphthalide 575-61-1
C15H10O2 Aurone 582-04-7
C15H10O2 Flavone
C15H10O2 Isoflavonoid
C15H10O2 Phenindione 83-12-5
C15H10O3 6-hydroxyflavone6665-83-4
C15H10O4 Chrysin – 480-40-0
C15H10O4 Daidzein – 486-66-8
C15H10O4 Hispidol
C15H10O4 Coumestrol – 479-13-0
C15H10O5 Fisetinidin – 2948-76-7
C15H10O5 Luteolinidin – 1154-78-5
C15H10O5 Pelargonidin – 134-04-3
C15H10O6 Apigenin – 520-36-5
C15H10O6 Aloe emodin - 481-72-1
C15H10O6 Baicalein - 491-67-8
C15H10O6 Emodin - 518-82-1
C15H10O6 Galangin - 548-83-4
C15H10O6 Genistein - 446-72-0
C15H10O6 Morindone - 478-29-5
C15H10O6 Thunberginol A - 147666-80-6
C15H10O6 Thunberginol F - 147666-82-8
C15H10O7 Several molecules
C15H10O8 Several molecules
C15H11ClN2O mecloqualone 340-57-8
C15H11ClN2O norchlordiazepoxide 16300-25-7
C15H11ClN2O nordazepam 1088-11-5
C15H11ClN2O2 demoxepam 963-39-3
C15H11ClN2O2 norclobazam 22316-55-8
C15H11ClN2O2 oxazepam 604-75-1
C15H11N3O daniquidone 67199-66-0
C15H11N3O3 nitrazepam 146-22-5
C15H11N3O7 indene picric acid 72454-47-8
C15H11O4 Apigeninidin
C15H11O4 Guibourtinidin
C15H11O5 Several molecules
C15H11O6 Several molecules
C15H11O7 Delphinidin13270-61-6
C15H12ClN3O desmethylchlordiazepoxide 7722-15-8
C15H12F9FeO6 ferric trifluoroacetylacetonate 14526-22-8
C15H12N2O carbamazepine 298-46-4
C15H12N2O tegretol 51-52-5
C15H12O benzalacetophenone 614-47-1
C15H12O2 phenylbenzylglyoxal 23464-17-7
C15H12O5 Several molecules
C15H12O6 Several molecules
C15H12O7 Several molecules
C15H12O8 Several molecules
C15H13ClN2 desmethylmedazepam 1694-78-6
C15H13F5OSi benzenemethanol dmpfps 71338-90-4
C15H13NO chalcone oxime 6502-38-1
C15H13N3O4S piroxicam 36322-90-4
C15H14ClN3O4S3 benzthiazide 91-33-8
C15H14N2O2 malonanilide 621-10-3
C15H14O Several molecules
C15H14O2 benzoin methyl ether 3524-62-7
C15H14O2 methyl diphenylacetate 3469-00-9
C15H14O3 dibenzyl carbonate 3459-92-5
C15H14O3 fenoprofen 31879-05-7
C15H14O3 methyl benzilate 76-89-1
C15H14O3 phenylethyl salicylate 87-22-9
C15H14O6 Several molecules
C15H15BrN2 nomelidine 60324-59-6
C15H15ClN2O2 chloroxuron 1982-47-4
C15H15NO dibenzyl ketoxime 1788-31-4
C15H15NO nordiphenamid 954-21-2
C15H15NO2 mefenamic acid 61-68-7
C15H15NO3 tolmetin 26171-23-3
C15H15OP allyldiphenylphosphine oxide 4141-48-4
C15H15P allyldiphenylphosphine 2741-38-0
C15H15Y tricyclopentadienyl yttrium 1294-07-1
C15H16 ditolylmethane 1335-47-3
C15H16Cl3N3O2 prochloraz 68444-81-5
C15H16N2O2 ancymidol 12771-68-5
C15H16O2 benzophenone dimethyl ketal 2235-01-0
C15H16O3 osthole 484-12-8
C15H16Si methyldiphenylvinylsilane 13107-13-6
C15H17Cl2N3O2 propiconazole 75881-82-2
C15H17N dibenzyl methyl amine 102-05-6
C15H18 tricyclopentabenzene 1206-79-7
C15H18Cl2N2O3 oxadiazon 19666-30-9
C15H19MnO2 cyclooctenecyclopentadienylmanganese dicarbonyl 49716-47-4
C15H19NO2 bisnortilidine 53948-51-9
C15H19NS2 ethylmethylthiambutene 441-61-2
C15H20N2O anagyrine 486-89-5
C15H20N2O rhombifoline 529-78-2
C15H20N2O thermopsine 486-90-8
C15H20N2S methaphenilene 493-78-7
C15H20O curzerene 17910-09-7
C15H20O4 butyl benzyl succinate 1223-37-6
C15H20O4 ethylphenylmalonic acid diethyl ester 76-67-5
C15H20O4 jesterone
C15H20O6 deoxynivalenol 51481-10-8
C15H21F3N2O2 fluvoxamine 54739-18-3
C15H21MnO6 manganic acetylacetonate 14284-89-0
C15H21N fencamfamin 1209-98-9
C15H21NO metazocine 3734-52-9
C15H21NO2 benzamine 500-34-5
C15H21NO2 ketobemidone 469-79-4
C15H21NO3 hydroxypethidine 468-56-4
C15H21N3O primaquine 90-34-6
C15H21N3O2 physostigmine 57-47-6
C15H21N3O3 eseridine 25573-43-7
C15H22ClNO2 metolachlor 51218-45-2
C15H22N2O carbocaine 96-88-8
C15H22N2O milnacipran 92623-85-3
C15H22N2O3 tolycaine 3686-58-6
C15H22O aristolone 6831-17-0
C15H22O curlone 87440-60-6
C15H22O dendrolasin 23262-34-2
C15H22O germacrone 6902-91-6
C15H22O nootcatane 4674-50-4
C15H22O solavetivone 54878-25-0
C15H22O xanthorrhizol 30199-26-9
C15H22O zerumbone 471-05-6
C15H22O2 davana ether 35470-57-6
C15H22O2 hexl dihydrocinnamate 220766-75-6
C15H22O2 phenylethyl heptanoate 5454-11-5
C15H22O10 arabitol pentaacetate 26674-23-7
C15H23ClO4S aramite 140-57-8
C15H23N prolintane 493-92-5
C15H23NO2 alprenolol 13655-52-2
C15H23NO3 oxprenolol 6452-71-7
C15H23N3O4 isopropalin 33820-53-0
C15H23N3O4S sulpiride 15676-16-1
C15H24 -chamigrene 18431-82-8
C15H24 acoradiene 24048-44-0
C15H24 aromadendrene 109119-91-7
C15H24 bicyclogermacrene 67650-90-2
C15H24 cedrene 11028-42-5
C15H24 clovene 469-92-1
C15H24 cyperene 2387-78-2
C15H24 elemene 11029-06-4
C15H24 eremophilene 10219-75-7
C15H24 germacrene a 28387-44-2
C15H24 germacrene b 15423-57-1
C15H24 longicyclene 1137-12-8
C15H24 patchoulene 1405-16-9
C15H24 seychellene 20085-93-2
C15H24 thujopsene 470-40-6
C15H24 viridiflorene 21747-46-6
C15H24N2O aphylline 577-37-7
C15H24N2O epiaphylline 1218-51-5
C15H24N2O lupanine 550-90-3
C15H24N2O trimecaine 616-68-2
C15H24N2O2 amethocaine 94-24-6
C15H24N2O2 hydroxylupanine 15358-48-2
C15H24N2O4S tiapride 51012-32-9
C15H24O butylated hydroxytoluene 128-37-0
C15H24O cedranone 13567-40-3
C15H24O cedrenol 28231-03-0
C15H24O longifolenaldehyde 19890-84-7
C15H24O nonyloxybenzene 36588-31-5
C15H24O nonylphenol 25154-52-3
C15H24O spathulenol 6750-60-3
C15H24O vetivenol 68129-81-7
C15H24O2 curdione 13657-68-6
C15H24O2 davanone 20482-11-5
C15H24O2 geranyl tiglate 7785-33-3
C15H24S nonylphenyl sulfide 500041-11-2
C15H25NO3 metoprolol 37350-58-6
C15H25NO3Si2 hippuric acid ditms 55133-85-2
C15H25NO4 supinine 551-58-6
C15H25NO5 echinatine 480-83-1
C15H25NO5 indicine 480-82-0
C15H25NO5 rinderine 6029-84-1
C15H25O3P dibutyl benzylphosphonate 3762-27-4
C15H26 cadinene 29350-73-0
C15H26 clovane 469-91-0
C15H26 patchoulane 25491-20-7
C15H26N2 sparteine 90-39-1
C15H26N2O retamine 2122-29-4
C15H26O agarospirol 1460-73-7
C15H26O bulnesol 22451-73-6
C15H26O carotol 465-28-1
C15H26O cedrol 77-53-2
C15H26O cubenol 21284-22-0
C15H26O drimenol 19078-37-6
C15H26O eudesmol 51317-08-9
C15H26O globulol 51371-47-2
C15H26O guaiol 489-86-1
C15H26O hedycaryol 21657-90-9
C15H26O himachalol 1891-45-8
C15H26O hinesol 23811-08-7
C15H26O juniper camphor 473-04-1
C15H26O juniperol 465-24-7
C15H26O ledol 577-27-5
C15H26O levomenol 23089-26-1
C15H26O patchouli alcohol 5986-55-0
C15H26O valeranone 1803-39-0
C15H26O viridiflorol 552-02-3
C15H26O widdrol 6892-80-4
C15H26O2 bisabolol oxide b 55399-12-7
C15H26O2 citronellyl tiglate 24717-85-9
C15H26O2 geranyl isovalerate 109-20-6
C15H26O2 geranyl valerate 10402-47-8
C15H26O2 linalyl valerate 10471-96-2
C15H26O4 ethylene brassylate 105-95-3
C15H26O6 tributyrin 60-01-5
C15H27Cl3O2 tridecyl trichloroacetate 74339-51-8
C15H27NO4 trachelanthamine 14140-18-2
C15H28 amorphane 34315-85-0
C15H28 muurolane 29788-41-8
C15H28 selinane 30824-81-8
C15H28O cyclopentadecanone 502-72-7
C15H28O dihydrofarnesol 1335-48-4
C15H28O2 citronellyl isovalerate 68922-10-1
C15H28O2 citronellyl valerate 7540-53-6
C15H28O2 dodecyl acrylate 2156-97-0
C15H28O2 menthyl valerate 64129-94-8
C15H28O2 pentadecanolide 32539-85-8
C15H28O4 diethyl octylmalonate 1472-85-1
C15H28O4 dodecylmalonic acid 4371-74-8
C15H28O4 monodecyl glutarate 97526-58-4
C15H29ClO pentadecanoyl chloride 17746-08-6
C15H29N pentadecanenitrile 18300-91-9
C15H29NS tetradecyl isothiocyanate 3224-48-4
C15H30 bisabolane 29799-19-7
C15H30 cyclopentadecane 295-48-7
C15H30O2 ethyl tridecanoate 28267-29-0
C15H30O2 heptyl caprylate 4265-97-8
C15H30O2 isopropyl laurate 10233-13-3
C15H30O2 pentadecanoic acid 1002-84-2
C15H30O2 propyl laurate 3681-78-5
C15H32 pentadecane 629-62-9
C15H32O3S tetradecyl methanesulfonate 6222-16-8
C15H32O4S pentadecyl sulfuric acid 45247-34-5
C15H32O6 pentapropylene glycol 21482-12-2
C15H32Sn allyltributyltin 24850-33-7
C15H33N methyltetradecylamine 29369-63-9
C15H33N pentadecylamine 2570-26-5
C15H33O4P tripentyl phosphate 2528-38-3
C15H35NO2Si2 alanine ditbdms 92751-15-0

See also


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<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, or olefin, 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.

A chemical element is a chemical substance that cannot be broken down into other substances by chemical reactions. The basic particle that constitutes a chemical element is the atom. Chemical elements are identified by the number of protons in the nuclei of their atoms, known as the element's atomic number. For example, oxygen has an atomic number of 8, meaning that each oxygen atom has 8 protons in its nucleus. Two or more atoms of the same element can combine to form molecules, in contrast to chemical compounds or mixtures, which contain atoms of different elements. Atoms can be transformed into different elements in nuclear reactions, which change an atom's atomic number.

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> Group of atoms giving a molecule characteristic 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> Carbon-containing chemical compound

Some chemical authorities define an organic compound as a chemical compound that contains a carbon–hydrogen or carbon–carbon bond; others consider an organic compound to be any chemical compound that contains carbon. For example, carbon-containing compounds such as alkanes and its derivatives are universally considered organic, but many others are sometimes 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> Chemical property

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.

<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.