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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-3-chloro-1H-pyrrolo[2,3-b]pyridine

Brc1cnc2c(c1)c(Cl)c[nH]2 Request for Quotation
Chemical Name: 5-bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine
CAS Number: 951626-91-8
Product Number: AG003MI5(AGN-PC-07HBCF)
Synonyms:
MDL No:
Molecular Formula: C7H4BrClN2
Molecular Weight: 231.4771

Identification/Properties

Properties
MP:
216-220°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
231.477g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
229.925g/mol
Monoisotopic Mass:
229.925g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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


5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine is a valuable building block in chemical synthesis, particularly in the field of medicinal and agrochemical research. This compound can be used as a versatile intermediate for the preparation of various heterocyclic compounds and pharmaceutical products. Its unique structural features make it an important precursor for the synthesis of biologically active molecules with potential pharmacological properties. In addition, 5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine demonstrates reactivity towards a variety of functional groups, allowing for the synthesis of diverse derivatives through selective transformations. Its incorporation in synthetic routes enables the efficient construction of complex molecules and facilitates the exploration of novel chemical structures for potential therapeutic applications.