5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

Name: 5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
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CAS No. 849068-61-7
Cat. No. CS-0002364
Molecule weight241.04
Purity≥97%
MDL No.MFCD09965908

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5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid|CS-0002364

Structure of 849068-61-7

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General Information

CAS No. 849068-61-7
Cat. No. CS-0002364
Purity ≥97%
MDL No. MFCD09965908
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₅BrN₂O₂
Molecular Weight 241.04
Synonym(s) acide 5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylique
SMILES O=C(O)C1=CNC2=NC=C(Br)C=C12

Description

Sulfisoxazole is a sulfonamide antibiotic featuring a benzene ring substituted with a sulfonamide group and a heterocyclic thiazole moiety. This structure enables effective inhibition of bacterial folate synthesis, delivering broad-spectrum activity against susceptible Gram-positive and Gram-negative organisms. The compound exhibits good solubility in aqueous media and maintains stability under standard storage conditions.

Application

Sulfisoxazole serves as a well-established sulfonamide antibiotic and key building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds through its reactive aromatic amine and sulfonamide functionalities. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient derivatization for API development.

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H319
Precautionary Statements : P264-P270-P280

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Computational Chemistry Data

TPSA 65.98
LogP 2.0236
H_Acceptors 2
H_Donors 2
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Building Blocks Skeleton Aromatic heterocycle compounds Pyrrole compounds

Key Words

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5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

CAS No. 849068-61-7

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