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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)-

2-chloro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine

COc1nc(Cl)nc2c1cc[nH]2 Request for Quotation
Chemical Name: 2-chloro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine
CAS Number: 96022-77-4
Product Number: AG01CB57(AGN-PC-05J2QT)
Synonyms:
MDL No:
Molecular Formula: C7H6ClN3O
Molecular Weight: 183.59504

Identification/Properties

Computed Properties
Molecular Weight:
183.595g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
183.02g/mol
Monoisotopic Mass:
183.02g/mol
Topological Polar Surface Area:
50.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
169
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


2-Chloro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine is a versatile compound widely utilized in chemical synthesis due to its unique chemical properties. It serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.One prominent application of 2-Chloro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine is in the pharmaceutical industry where it is employed as a precursor in the synthesis of biologically active compounds. Its structure allows for the introduction of functional groups at different positions, making it an essential intermediate in the production of diverse drug molecules.Furthermore, this compound is also utilized in the synthesis of complex organic molecules, specifically in the formation of heterocyclic compounds. The presence of the chloro and methoxy substituents on the pyrrolopyrimidine ring makes it a valuable starting material for creating novel chemical structures with potential applications in various fields.Overall, 2-Chloro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine plays a crucial role in chemical synthesis by enabling the construction of intricate molecular frameworks with desired properties for pharmaceutical, agrochemical, and material science applications.