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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(3-OXOCYCLOHEXYL)ACETIC ACID

OC(=O)CC1CCCC(=O)C1 Request for Quotation
Chemical Name: 2-(3-OXOCYCLOHEXYL)ACETIC ACID
CAS Number: 39762-51-1
Product Number: AG01DWEI(AGN-PC-0WAJ1M)
Synonyms:
MDL No:
Molecular Formula: C8H12O3
Molecular Weight: 156.1791

Identification/Properties

Computed Properties
Molecular Weight:
156.181g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
156.079g/mol
Monoisotopic Mass:
156.079g/mol
Topological Polar Surface Area:
54.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
174
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Oxocyclohexyl)acetic acid, also known as keto-adipic acid, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in various organic reactions due to its unique structural properties and functional groups. In organic synthesis, 2-(3-Oxocyclohexyl)acetic acid can be utilized as a precursor for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.One of the prominent applications of 2-(3-Oxocyclohexyl)acetic acid is in the synthesis of heterocyclic compounds. By incorporating this compound into the reaction, chemists can access a diverse range of heterocycles, which are essential structural motifs found in many biologically active molecules. Moreover, the keto group in 2-(3-Oxocyclohexyl)acetic acid can undergo a variety of transformations, such as reduction or oxidation, leading to the generation of new compounds with tailored properties.Furthermore, 2-(3-Oxocyclohexyl)acetic acid can also be used in the preparation of chiral molecules. Its cyclohexyl ring provides a stereochemical framework that can be selectively modified to introduce chirality into the molecule. This feature is crucial in the synthesis of enantiomerically pure compounds, which are essential in the pharmaceutical industry for enhancing biological activity and reducing side effects.Overall, the versatile nature of 2-(3-Oxocyclohexyl)acetic acid makes it a valuable tool in chemical synthesis, offering multiple avenues for creating complex organic molecules with diverse applications in various industries.