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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)-

6-chloro-4-methoxypyridine-3-carbonitrile

COc1cc(Cl)ncc1C#N Request for Quotation
Chemical Name: 6-chloro-4-methoxypyridine-3-carbonitrile
CAS Number: 1187190-69-7
Product Number: AG0035ZV(AGN-PC-0AC0YF)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2O
Molecular Weight: 168.5804

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
168.58g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
168.009g/mol
Monoisotopic Mass:
168.009g/mol
Topological Polar Surface Area:
45.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
177
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-CHLORO-4-METHOXYNICOTINONITRILE is a valuable chemical intermediate commonly used in organic synthesis. This compound serves as a versatile building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique molecular structure allows for selective functionalization and modification, making it an essential component in the synthesis of diverse molecular entities. In chemical synthesis, 6-CHLORO-4-METHOXYNICOTINONITRILE plays a crucial role as a key starting material for the preparation of complex molecules with specific biological activities or properties. Its presence enables the creation of novel compounds through strategic transformations and derivatizations, contributing to the advancement of drug discovery and material science.