1. Home
  2. methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

COC(=O)c1[nH]c2c(c1Br)cccn2 Request for Quotation
Chemical Name: methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
CAS Number: 913181-71-2
Product Number: AG00IGL5(AGN-PC-079H3A)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2O2
Molecular Weight: 255.06808

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate is a valuable intermediate in chemical synthesis due to its versatility and unique structural features. This compound serves as a key building block in the preparation of various biologically active molecules, pharmaceuticals, and agrochemicals. Its functional groups offer multiple opportunities for further derivatization, enabling the creation of diverse chemical libraries and novel compounds. In particular, the presence of the pyrrolopyridine core in this compound enhances its potential for use in drug discovery and development efforts targeting diseases such as cancer, inflammation, and neurological disorders. Its incorporation into molecular scaffolds can lead to the modulation of specific biological targets, making it an essential tool in the design and optimization of new therapeutic agents. Additionally, the selective bromination at the 3-position provides a valuable handle for subsequent transformations, facilitating the construction of complex molecular architectures with high efficiency and precision.