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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)-

4-Bromo-6-Chloro-1H-Pyrrolo[2,3-b]Pyridine

Clc1cc(Br)c2c(n1)[nH]cc2 Request for Quotation
Chemical Name: 4-Bromo-6-Chloro-1H-Pyrrolo[2,3-b]Pyridine
CAS Number: 942920-50-5
Product Number: AG006C7S(AGN-PC-04Q69N)
Synonyms:
MDL No:
Molecular Formula: C7H4BrClN2
Molecular Weight: 231.4771

Identification/Properties

Properties
BP:
359.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
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:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrrolo[2,3-b]pyridine, 4-bromo-6-chloro- is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and materials. Its unique structure allows for diverse functionalization and modification, making it a key intermediate in the creation of complex organic molecules. When incorporated into synthetic routes, 1H-Pyrrolo[2,3-b]pyridine, 4-bromo-6-chloro- enables chemists to introduce specific functionalities and stereochemistries into their target molecules efficiently. Known for its stability and reactivity, this compound plays a crucial role in the development of novel compounds with potential applications across different industries.