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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-(4,4-difluorocyclohexyl)acetonitrile

N#CCC1CCC(CC1)(F)F Request for Quotation
Chemical Name: 2-(4,4-difluorocyclohexyl)acetonitrile
CAS Number: 959600-88-5
Product Number: AG00IJOF(AGN-PC-0H6TO6)
Synonyms:
MDL No:
Molecular Formula: C8H11F2N
Molecular Weight: 159.1764

Identification/Properties

Computed Properties
Molecular Weight:
159.18g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
159.086g/mol
Monoisotopic Mass:
159.086g/mol
Topological Polar Surface Area:
23.8A^2
Heavy Atom Count:
11
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


2-(4,4-Difluorocyclohexyl)acetonitrile, also known as $name$, is a versatile compound widely used in chemical synthesis. This organic compound plays a crucial role as a building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and functional groups, $name$ acts as a key intermediate in the synthesis of complex molecules by facilitating key reactions such as nucleophilic additions, substitutions, and transformations. Its incorporation in organic reactions enables the formation of diverse chemical bonds, leading to the production of novel molecules with valuable properties. Chemical researchers and synthetic chemists leverage the reactivity and selectivity of 2-(4,4-Difluorocyclohexyl)acetonitrile to craft innovative compounds with potential applications in drug discovery, material science, and advanced technologies.