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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)-

1H-Pyrrolo[2,3-b]pyridine, 5-bromo-6-chloro-

Brc1cc2cc[nH]c2nc1Cl Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 5-bromo-6-chloro-
CAS Number: 1190321-59-5
Product Number: AG000HZY(AGN-PC-09RUVG)
Synonyms:
MDL No:
Molecular Formula: C7H4BrClN2
Molecular Weight: 231.4771

Identification/Properties

Computed Properties
Molecular Weight:
231.477g/mol
XLogP3:
3
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

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-6-chloro-1H-pyrrolo[2,3-b]pyridine is a versatile building block in chemical synthesis, particularly in the field of medicinal chemistry. This compound is commonly used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity. Its bromo and chloro substituents make it a valuable precursor for introducing functional groups into organic molecules through cross-coupling reactions, Suzuki-Miyaura couplings, and other palladium-catalyzed transformations. Additionally, the pyrrolopyridine scaffold is found in many bioactive compounds, making 5-Bromo-6-chloro-1H-pyrrolo[2,3-b]pyridine an essential building block for designing novel drug candidates with potential therapeutic applications.