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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)-

Pyrimidine, 4-chloro-6-[(phenylmethoxy)methyl]-

Clc1ncnc(c1)COCc1ccccc1 Request for Quotation
Chemical Name: Pyrimidine, 4-chloro-6-[(phenylmethoxy)methyl]-
CAS Number: 914802-11-2
Product Number: AG006A6K(AGN-PC-09S100)
Synonyms:
MDL No:
Molecular Formula: C12H11ClN2O
Molecular Weight: 234.6815

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-((Benzyloxy)methyl)-6-chloropyrimidine is a versatile compound widely used in chemical synthesis as a key building block. Its unique structure contains a benzyloxy group attached to the methyl carbon of the pyrimidine ring, providing a site for further functionalization. This compound is particularly valuable in organic chemistry reactions, serving as a precursor in the synthesis of various biologically active molecules and pharmaceutical intermediates. Its ability to undergo a range of transformations, such as N-alkylation, cross-coupling reactions, and substitution reactions, makes it an essential tool for the preparation of complex organic compounds. Additionally, the presence of the chloro group enhances reactivity and enables selective modifications, making 4-((Benzyloxy)methyl)-6-chloropyrimidine a valuable asset in the toolkit of synthetic chemists.