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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-Pyridinecarbonitrile, 5-chloro-3-methyl-

N#Cc1ncc(cc1C)Cl Request for Quotation
Chemical Name: 2-Pyridinecarbonitrile, 5-chloro-3-methyl-
CAS Number: 156072-84-3
Product Number: AG001OHM(AGN-PC-03GV2T)
Synonyms:
MDL No: MFCD17214209
Molecular Formula: C7H5ClN2
Molecular Weight: 152.5810

Identification/Properties

Computed Properties
Molecular Weight:
152.581g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
152.014g/mol
Monoisotopic Mass:
152.014g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
160
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


5-Chloro-2-cyano-3-methylpyridine is a versatile chemical compound widely used in various chemical synthesis processes. Due to its unique molecular structure, this substance serves as a valuable building block in the creation of numerous organic compounds, particularly in the field of medicinal chemistry. In chemical synthesis, 5-Chloro-2-cyano-3-methylpyridine functions as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its reactivity allows for the formation of complex structures through functional group transformations and carbon-carbon bond formations. Additionally, this compound plays a crucial role in the development of new materials, such as dyes, pigments, and polymers. Its presence in the synthetic chemistry toolkit enables the construction of diverse molecular architectures with tailored properties and functionalities.Overall, the application of 5-Chloro-2-cyano-3-methylpyridine in chemical synthesis showcases its significance in creating innovative compounds with potential applications across various industries.