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

Clc1c[nH]c2c1c(Br)ccn2 Request for Quotation
Chemical Name: 4-bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine
CAS Number: 943323-92-0
Product Number: AG00H8G4(AGN-PC-07HBAK)
Synonyms:
MDL No:
Molecular Formula: C7H4BrClN2
Molecular Weight: 231.4771

Identification/Properties

Properties
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine is a versatile building block in chemical synthesis, known for its unique structural properties that make it a valuable tool in the development of various organic compounds. This compound is commonly used in the pharmaceutical industry for the synthesis of novel drug candidates due to its ability to introduce both bromine and chlorine functionalities into complex molecules. Additionally, its fused pyrrolopyridine framework imparts desirable electronic and steric effects, making it an ideal starting material for creating diverse chemical structures. In organic synthesis, 4-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine is employed as a key intermediate in the preparation of heterocyclic compounds with potential biological activity, offering chemists a powerful tool for designing and accessing new molecules with tailored properties.