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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)-

5-bromo-4-chloro-7-methylpyrrolo[2,3-d]pyrimidine

Cn1cc(c2c1ncnc2Cl)Br Request for Quotation
Chemical Name: 5-bromo-4-chloro-7-methylpyrrolo[2,3-d]pyrimidine
CAS Number: 1266343-30-9
Product Number: AG000T0K(AGN-PC-0H0HBG)
Synonyms:
MDL No:
Molecular Formula: C7H5BrClN3
Molecular Weight: 246.4917

Identification/Properties

Computed Properties
Molecular Weight:
246.492g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
244.936g/mol
Monoisotopic Mass:
244.936g/mol
Topological Polar Surface Area:
30.7A^2
Heavy Atom Count:
12
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-4-chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine is a versatile chemical compound that finds wide application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structure and reactivity.One of the primary applications of 5-Bromo-4-chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine is in the synthesis of novel heterocyclic compounds with biological activity. Its substituted pyrrolopyrimidine core provides a solid foundation for the development of potential drug candidates. By incorporating this compound into the molecular structure of new compounds, chemists can explore the potential pharmacological properties of the resulting molecules.Furthermore, 5-Bromo-4-chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine can also be used as a linker or coupling agent in organic synthesis. Its bromo and chloro functionalities allow for further derivatization and modification, enabling the attachment of various functional groups to tailor the compound for specific applications. This flexibility makes it a valuable tool in the construction of complex molecules in medicinal chemistry and material science.Overall, the versatility and reactivity of 5-Bromo-4-chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine make it a valuable asset in chemical synthesis, particularly in the development of bioactive compounds and advanced materials.