91983-14-1

Basic information

• Product Name: 2-Bromomethylphenylboronic acid
• Synonyms: RARECHEM AH PB 0060;2-(BROMOMETHYL)BENZENEBORONIC ACID;2-BROMOMETHYLPHENYLBORONIC ACID;2-Boronobenzyl bromide;2-Bromomethylphenylboronic;2-(Bromomethyl)benzeneboronic acid 95%;2-(BroMoMethyl)phenylboronic Acid (contains varying aMounts of Anhydride);2-BroMoMethylphenylb
• CAS NO: 91983-14-1
• Molecular Formula: C₇H₈BBrO₂
• Molecular Weight: 214.85
• EINECS: 1308068-626-2
• Product Categories: blocks;BoronicAcids;Bromides;Boronic acids;Heterocyclic Compounds;Aryl;Organoborons;Boronic Acids;Boronic Acids and Derivatives
• Mol File: 91983-14-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 145-148
• Boiling Point: 358.5 ºC at 760 mmHg
• Flash Point: 170.6 ºC
• Appearance: /
• Density: 1.57 g/cm³
• Vapor Pressure: 9.22E-06mmHg at 25°C
• Refractive Index: 1.582
• Storage Temp.: 2-8°C
• PKA: 8.44±0.58(Predicted)
• CAS DataBase Reference: 2-Bromomethylphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromomethylphenylboronic acid(91983-14-1)
• EPA Substance Registry System: 2-Bromomethylphenylboronic acid(91983-14-1)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-20/21/22
• Safety Statements: 26-36/37/39-36/37-36
• RIDADR: 3261
• WGK Germany: 3
• HazardClass: IRRITANT
• PackingGroup: III
• Hazardous Substances Data: 91983-14-1(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 91983-14-1 differently. You can refer to the following data:
1. suzuki reaction
2. Reactant involved in:Studies of carbon-boron bond cleavage of phenylboronate-pendant cyclenDevelopment of a sensory system to detect glucose or other monosaccharides and hydroxycarboxylatesSynthesis of boronated triaryl and tetraaryl phosphonium salts used in cytotoxicity studiesColorimetry and fluorometry mercury determination with chemosensors composed of rhodamine and boronic acid groupsSynthesis of imidazolium-containing boronic acids used as fluoride ion sensorsReactions with adenine for molecules with antiinflammatory antitumor activities?

InChI:InChI=1/C7H8BBrO2/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,10-11H,5H2

Upstream product

• 16419-60-6 2-Methylphenylboronic acid 
• 95-46-5 2-methylphenyl bromide 
• 128-08-5 N-Bromosuccinimide 

Downstream Products

• 5735-41-1 3H-benzo[c][1,2]oxaborol-1-ol 
• 745835-05-6 2-(azidomethyl)phenylboronic acid 
• 909804-24-6 (2-{[(2-tert-butoxycarbonylamino-ethyl)-methyl-amino]-methyl}-phenyl)-boronic acid 
• 909804-19-9 (2-{[(3-tert-butoxycarbonylamino-propyl)-methyl-amino]-methyl}-phenyl)-boronic acid 
• 4261-14-7 9-benzyl-9H-purin-6-ylamine 
• 7481-16-5 2,4,6-Tris[o-(bromomethyl)phenyl]boroxine 
• 209396-01-0 1-(N-methyl-N-(o-boronobenzyl))aminomethylbenzene 

Relevant articles and documents

Method for analysis of different oligosacchiride structures

In this study, an improved, rapid, high yield synthesis of N,N'-4,4'-bis(benzyl-2-boronic acid)-bipyridinium dibromide (o-BBV) is described. The obtained o-BVV is applied in a two-component saccharide sensing system (complex) where it serves as a fluoresc

Efficient one-step synthesis and properties of photochromic diarylethenes having an indene bridging unit

Two novel isomeric photochromic diarylethenes with an indene bridging unit have been prepared by a simple and efficient one-step synthesis method. Their properties, including photochromic behavior, fluorescent properties and fatigue resistance, have been

Synthesis of (azidomethyl)phenylboronic acids

The synthesis of 2-, 3-, and 4-(azidomethyl)phenylboronic acids was carried out. The geometric and electronic structures were studied by quantum-chemical methods. The suggestion is made that there are weak intramolecular interactions between the boron atom and the nitrene nitrogen atom of the azido group.