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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)-

[1,1'-Bicyclohexyl]-4-one

O=C1CCC(CC1)C1CCCCC1 Request for Quotation
Chemical Name: [1,1'-Bicyclohexyl]-4-one
CAS Number: 92-68-2
Product Number: AG00626B(AGN-PC-0JKS8O)
Synonyms:
MDL No:
Molecular Formula: C12H20O
Molecular Weight: 180.2866

Identification/Properties

Properties
MP:
29.2℃
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
180.291g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
180.151g/mol
Monoisotopic Mass:
180.151g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
170
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of [1,1'-Bi(cyclohexan)]-4-one in chemical synthesis is particularly significant in asymmetric catalysis. This compound, also known as "Duanephos," serves as an effective ligand in various catalytic reactions due to its chiral structure. By coordinating with transition metal catalysts, [1,1'-Bi(cyclohexan)]-4-one can facilitate enantioselective transformations, allowing for the production of chiral molecules with high optical purity. Its utility extends to a wide range of organic reactions, including asymmetric hydrogenation, hydroformylation, and allylic substitution. The unique stereochemical properties of [1,1'-Bi(cyclohexan)]-4-one make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.