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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-(4-bromopyridin-2-yl)cyclopropane-1-carbonitrile

N#CC1(CC1)c1nccc(c1)Br Request for Quotation
Chemical Name: 1-(4-bromopyridin-2-yl)cyclopropane-1-carbonitrile
CAS Number: 1163707-56-9
Product Number: AG000CBG(AGN-PC-0BSZRH)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2
Molecular Weight: 223.0693

Identification/Properties

Computed Properties
Molecular Weight:
223.073g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
221.979g/mol
Monoisotopic Mass:
221.979g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
226
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Bromopyridin-2-yl)cyclopropanecarbonitrile is a versatile compound that plays a crucial role in chemical synthesis processes. This compound is widely utilized as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable building block for creating complex organic molecules with diverse applications.In chemical synthesis, 1-(4-Bromopyridin-2-yl)cyclopropanecarbonitrile can be employed in the construction of heterocyclic compounds through cycloaddition reactions. Additionally, its functional groups can be manipulated to introduce different substituents, allowing for the generation of structurally diverse compounds. This compound's presence in the synthesis pathway can impart desired biological activities or chemical properties to the final product, making it an essential component in the development of new materials and compounds.