4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine

Name: 4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine
Brand: ChemScene
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CAS No. 1369326-01-1
Cat. No. CS-0050977
Purity≥97%
MDL No.None

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4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine|CS-0050977

Structure of 1369326-01-1

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General Information

CAS No. 1369326-01-1
Cat. No. CS-0050977
Purity ≥97%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₆BrN₃
Molecular Weight 212.05
Synonym(s) None
SMILES CC1=CC(Br)=C2C=NNC2=N1

Description

4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine is a heterocyclic scaffold featuring a brominated pyrazolopyridine core with a methyl group at the 6-position. This electron-deficient system facilitates efficient coupling reactions in cross-coupling and medicinal chemistry applications. The molecule exhibits bench-stable handling properties and integrates readily into complex molecular architectures.

Application

4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its bromine at C4 enables palladium-catalyzed cross-coupling reactions, while the methyl group at C6 enhances solubility and modulates electronic properties. The pyrazolopyridine core provides robust bench stability and compatibility with diverse functional groups, facilitating rapid access to complex scaffolds via standard coupling protocols.

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-H312-H315-H319-H332-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501

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Computational Chemistry Data

TPSA 41.57
LogP 2.02882
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 0

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Building Blocks Skeleton Aromatic heterocycle compounds Pyrazole compounds

Key Words

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4-Bromo-6-methyl-1H-pyrazolo[3,4-b]pyridine

CAS No. 1369326-01-1

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