1. Home
  2. Pyrimidine, 2-chloro-4-methyl-6-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Pyrimidine, 2-chloro-4-methyl-6-phenyl-

Cc1nc(Cl)nc(c1)c1ccccc1 Request for Quotation
Chemical Name: Pyrimidine, 2-chloro-4-methyl-6-phenyl-
CAS Number: 32785-40-3
Product Number: AG00CNGP(AGN-PC-0C8DTV)
Synonyms:
MDL No:
Molecular Formula: C11H9ClN2
Molecular Weight: 204.6556

Identification/Properties

Computed Properties
Molecular Weight:
204.657g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
204.045g/mol
Monoisotopic Mass:
204.045g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
180
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-4-methyl-6-phenylpyrimidine is a versatile compound that plays a crucial role in chemical synthesis applications. Its unique chemical structure and reactivity make it an important building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. This compound is commonly used as a key intermediate in the synthesis of biologically active molecules due to its ability to undergo multiple types of reactions, such as nucleophilic substitution, transition metal-catalyzed coupling, and cyclization reactions. In addition, 2-Chloro-4-methyl-6-phenylpyrimidine is favored by synthetic chemists for its high selectivity and efficiency in forming complex molecular structures, making it an indispensable tool in the development of new compounds with potential therapeutic or agricultural benefits.