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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)-

methyl 2-(6-chloropyrimidin-4-yl)acetate

COC(=O)Cc1cc(Cl)ncn1 Request for Quotation
Chemical Name: methyl 2-(6-chloropyrimidin-4-yl)acetate
CAS Number: 1097779-00-4
Product Number: AG003RKX(AGN-PC-07YJZB)
Synonyms:
MDL No:
Molecular Formula: C7H7ClN2O2
Molecular Weight: 186.5957

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;
Computed Properties
Molecular Weight:
186.595g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
186.02g/mol
Monoisotopic Mass:
186.02g/mol
Topological Polar Surface Area:
52.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
166
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


Methyl 2-(6-chloropyrimidin-4-yl)acetate, a versatile compound commonly employed in chemical synthesis, serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Due to its unique structural features, this compound enables the introduction of the pyrimidine ring system into target molecules, thereby conferring specific biological activities or desired properties. Through strategic manipulation of its functional groups, researchers can facilely access a diverse array of derivatives, each possessing distinct reactivity profiles for further elaboration. The use of Methyl 2-(6-chloropyrimidin-4-yl)acetate in chemical transformations enables efficient access to structurally complex molecules and facilitates the synthesis of novel compounds with potential therapeutic or industrial applications.