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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)-

ethyl 3-cyclohexyl-3-oxopropanoate

CCOC(=O)CC(=O)C1CCCCC1 Request for Quotation
Chemical Name: ethyl 3-cyclohexyl-3-oxopropanoate
CAS Number: 15971-92-3
Product Number: AG001RD1(AGN-PC-0JNZTE)
Synonyms:
MDL No: MFCD04115574
Molecular Formula: C11H18O3
Molecular Weight: 198.2588

Identification/Properties

Properties
BP:
275.2°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
1.4630 to 1.4670
Computed Properties
Molecular Weight:
198.262g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
198.126g/mol
Monoisotopic Mass:
198.126g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
205
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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


Containing the structural elements of both a cyclohexane ring and an ester group, Ethyl 3-cyclohexyl-3-oxopropionate serves as a versatile building block in chemical synthesis. This compound is commonly utilized in the preparation of various organic molecules through esterification, reduction, and other synthetic transformations. Its unique structure allows for the introduction of both a cyclohexyl moiety and a carbonyl group into target molecules, enabling the modification and diversification of chemical structures for a wide range of applications in pharmaceuticals, agrochemicals, and materials science. Ethyl 3-cyclohexyl-3-oxopropionate's reactivity and functionality make it a valuable intermediate in the synthesis of complex organic compounds with tailored properties and functionalities. Its compatibility with various reaction conditions and functional group manipulations further highlight its utility in the creation of novel chemical entities with diverse biological and physical attributes.