5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine

Name: 5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine
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CAS No. 1934533-59-1
Cat. No. CS-0490857
Purity≥98%
MDL No.MFCD28656741

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5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine|CS-0490857

Structure of 1934533-59-1

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General Information

CAS No. 1934533-59-1
Cat. No. CS-0490857
Purity ≥98%
MDL No. MFCD28656741
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₆BrN₃
Molecular Weight 212.05
Synonym(s) None
SMILES CC1C(Br)=CC2C(=NNC=2)N=1

Description

5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine features a fused heterocyclic core with bromo and methyl substituents enabling direct functionalization in cross-coupling reactions. This bench-stable scaffold integrates readily into medicinal chemistry libraries, offering enhanced solubility and metabolic stability for target-oriented synthesis.

Application

5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances solubility and modulates electronic properties. The scaffold exhibits bench stability and compatibility with standard synthetic protocols, facilitating efficient access to complex pyrazolopyridine derivatives.

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-H315-H319-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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5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine

CAS No. 1934533-59-1

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