1223598-41-1

Basic information

• Product Name: 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%
• Synonyms: 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%;2-(2-(Azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 1223598-41-1
• Molecular Formula: C₁₃H₁₈BN₃O₂
• Molecular Weight: 277.1272
• Mol File: 1223598-41-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%(1223598-41-1)
• EPA Substance Registry System: 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%(1223598-41-1)

Safety Data

• Hazardous Substances Data: 1223598-41-1(Hazardous Substances Data)

Usage

Purity

95%

Type

Chemical compound

Usage

Commonly used in organic synthesis

Derivative

Boronic acid pinacol ester derivative

Applications

Suzuki-Miyaura cross-coupling reaction, preparation of pharmaceuticals, agrochemicals, and materials

Importance

Valuable tool for chemists and researchers in organic synthesis and molecular biology

Structure

Contains an azide group (-N3) attached to a benzene ring, with a boronic acid pinacol ester group attached to the benzene ring as well.

Upstream product

• 377780-72-8 2-(2-(bromomethyl)phenyl)-4,4,5,5,-tetramethyl-1,3,2-dioxaborolane 
• 195062-59-0 2-methylphenylboronic acid pinacol ester 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 16419-60-6 2-Methylphenylboronic acid 

Downstream Products

• 1020152-73-1 4-phenyl-1-(2-(4,4,5,5-tetramethyl-1,3,2-dioxabololan-2-yl)benzyl)-1H-1,2,3-triazole 
• 1284215-88-8 (CH₃(CH₂)9O)2C₆H₂(CCC₆H₂(O(CH₂)9CH₃)2C₂HN₃CH₂C₆H₄B(O₂C₂(CH₃)4))2 
• 1223598-43-3 C₅₄H₅₆B₂N₆O₄S₈ 

Relevant articles and documents

Glucose selective bis-boronic acid click-fluor

Four novel bis-boronic acid compounds were synthesised via copper catalysed azide-alkyne cycloaddition (CuAAC) reactions. Glucose selectivity was observed for a particular structural motif. Moreover, a new glucose selective fluorescent sensor was designed

PHARMACEUTICALLY ACTIVE PYRAZOLO-TRIAZINE AND/OR PYRAZOLO-PYRIMIDINE DERIVATIVES

The present invention relates to pyrazolo [1,5 -a] [1,3,5 ]triazine and pyrazolo[1,5-a] pyrimidine derivatives and/or pharmaceutically acceptable salts thereof, the use of these derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferative diseases, inflammatory diseases, immunological diseases, cardiovascular diseases and infectious diseases. Furthermore, the present invention is directed towards pharmaceutical compositions containing at least one of the pyrazo lo [1,5-a][1,3,5 ]triazine and pyrazolo [1,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof.