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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-2-methylpyrimidine-4-carbonitrile

N#Cc1cc(Cl)nc(n1)C Request for Quotation
Chemical Name: 6-chloro-2-methylpyrimidine-4-carbonitrile
CAS Number: 1192064-60-0
Product Number: AG000IDQ(AGN-PC-0WAM0L)
Synonyms:
MDL No:
Molecular Formula: C6H4ClN3
Molecular Weight: 153.5691

Identification/Properties

Computed Properties
Molecular Weight:
153.569g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
153.009g/mol
Monoisotopic Mass:
153.009g/mol
Topological Polar Surface Area:
49.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
162
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


6-chloro-2-methylpyrimidine-4-carbonitrile serves as a versatile building block in chemical synthesis, particularly within the realm of pharmaceutical and agrochemical industries. Through careful manipulation of its molecular structure, this compound can be utilized to introduce essential functional groups into complex organic molecules. Its strategic placement of a cyano group offers a valuable tool for the creation of heterocyclic scaffolds, which are prevalent in drug discovery and development. This compound's reactivity and compatibility with various reaction conditions make it an indispensable asset in the synthesis of novel compounds with potential biological activities. Additionally, its chloro and methyl substituents provide opportunities for further derivatization, allowing for the fine-tuning of properties such as solubility, stability, and bioavailability in target molecules. The application of 6-chloro-2-methylpyrimidine-4-carbonitrile in chemical synthesis underscores its significance as a key intermediate in the creation of diverse and valuable chemical compounds.