2-(Bromomethyl)phenylboronic acid

• Catalog No.: 679453
• CAS Number: 91983-14-1
• M. F.: C7H8BBrO2
• M. W.: 214.85222

SYNONYMS

• Title: 2-(溴甲基)苯硼酸
• IUPAC name: [2-(bromomethyl)phenyl]boronic acid
• IUPAC Traditional name: 2-(bromomethyl)phenylboronic acid
• Synonyms: o-Boronobenzyl bromide; α-Bromo-o-tolueneboronic acid

DATABASE IDS

• CAS Number: 91983-14-1
• MDL Number: MFCD01318941
• PubChem SID: 24885495

PROPERTIES

• Empirical Formula (Hill Notation): C7H8BBrO2
• Melting Point: 158-162 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36/37
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

General description
May contain varying amounts of anhydride.
Packaging
1, 5 g in glass bottle
Application
Reactant involved in:
• Studies of carbon-boron bond cleavage of phenylboronate-pendant cyclen1
• Development of a sensory system to detect glucose2,3 or other monosaccharides and hydroxycarboxylates4
• Synthesis of boronated triaryl and tetraaryl phosphonium salts used in cytotoxicity studies5
• Colorimetry and fluorometry mercury determination with chemosensors composed of rhodamine and boronic acid groups6
• Synthesis of imidazolium-containing boronic acids used as fluoride ion sensors7
• Reactions with adenine for molecules with antiinflammatory antitumor activities 8

Description (简体中文)

General description
可能含不定量的酸酐。
包装
1, 5 g in glass bottle
Application
Reactant involved in:
• Studies of carbon-boron bond cleavage of phenylboronate-pendant cyclen1
• Development of a sensory system to detect glucose2,3 or other monosaccharides and hydroxycarboxylates4
• Synthesis of boronated triaryl and tetraaryl phosphonium salts used in cytotoxicity studies5
• Colorimetry and fluorometry mercury determination with chemosensors composed of rhodamine and boronic acid groups6
• Synthesis of imidazolium-containing boronic acids used as fluoride ion sensors7
• Reactions with adenine for molecules with antiinflammatory antitumor activities 8