(3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)boronic acid

Name: (3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)boronic acid
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CAS No. 2377610-54-1
Cat. No. CS-0149309
Molecule weightNone
Purity≥95%
MDL No.MFCD22398789

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(3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)boronic acid|CS-0149309

Structure of 2377610-54-1

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General Information

CAS No. 2377610-54-1
Cat. No. CS-0149309
Purity ≥95%
MDL No. MFCD22398789
Storage -20°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₈BN₃O₂
Molecular Weight None
Synonym(s) {3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl}boronic acid
SMILES OB(C1=CN=C(NN=C2C)C2=C1)O

Description

This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The 3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl scaffold provides enhanced stability and solubility under standard conditions, facilitating robust reaction outcomes in complex molecular settings.

Application

(3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)boronic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its boronic acid functionality enables reliable Suzuki-Miyaura cross-coupling reactions under mild conditions, facilitating the assembly of complex aryl and heteroaryl architectures. The molecule exhibits good bench stability, ease of purification, and tolerance to various functional groups, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.

Safety Information

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Computational Chemistry Data

TPSA 82.03
LogP -1.05388
H_Acceptors 4
H_Donors 3
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Building Blocks Skeleton Aromatic heterocycle compounds Pyrazole compounds

Key Words

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(3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)boronic acid

CAS No. 2377610-54-1

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