1. Home
  2. Cyclohexanecarbonitrile, 4-oxo-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Cyclohexanecarbonitrile, 4-oxo-

N#CC1CCC(=O)CC1 Request for Quotation
Chemical Name: Cyclohexanecarbonitrile, 4-oxo-
CAS Number: 34916-10-4
Product Number: AG003LY4(AGN-PC-0NI6SD)
Synonyms:
MDL No: MFCD11847831
Molecular Formula: C7H9NO
Molecular Weight: 123.1525

Identification/Properties

Properties
BP:
271°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
123.155g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
123.068g/mol
Monoisotopic Mass:
123.068g/mol
Topological Polar Surface Area:
40.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
155
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Oxocyclohexanecarbonitrile is a versatile compound used in chemical synthesis as a key building block for various organic reactions. Its unique structure and reactivity make it an essential reagent in the production of pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of 4-Oxocyclohexanecarbonitrile is as a precursor in the synthesis of heterocyclic compounds, which are important in drug discovery and development. By reacting with a variety of nucleophiles, this compound can undergo diverse transformations to yield a range of valuable intermediates with potential biological activity.Additionally, 4-Oxocyclohexanecarbonitrile can participate in multicomponent reactions, enabling the efficient construction of complex molecular architectures in a single step. This property makes it particularly useful in the rapid assembly of drug-like molecules and natural product derivatives.Furthermore, the cyano group present in 4-Oxocyclohexanecarbonitrile can serve as a versatile handle for further functionalization, allowing for the introduction of additional functionality or stereochemical diversity in the final product. This flexibility enhances the molecule's utility in the synthesis of advanced intermediates for various applications in the chemical industry.