1-Phenylvinylboronic acid

• Catalog No.: 571350
• CAS Number: 14900-39-1
• M. F.: C8H9BO2
• M. W.: 147.96686
• Purity: 95%

SYNONYMS

• Title: 1-苯基乙烯基硼酸
• IUPAC name: (1-phenylethenyl)boronic acid
• IUPAC Traditional name: 1-phenylethenylboronic acid
• Synonyms: α-Phenyl vinylboronic acid; Styrene α-boronic acid; α-Methylene-α-tolueneboronic acid; (1-Phenylethenyl)boronic acid; α-苯基乙烯基硼酸

DATABASE IDS

• PubChem SID: 24880629
• CAS Number: 14900-39-1
• MDL Number: MFCD01074578

PROPERTIES

• Linear Formula: C6H5C=CH2B(OH)2
• Purity: 95%
• Melting Point: 125 °C (dec.)(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant involved in:
• Halogenation of alkynes for preparation of enol esters1
• Liebeskind-Srogl cross-coupling2
• Homocoupling of arylboronic acids for synthesis of biaryls3
• Iterative cross-coupling of boronate building blocks4
• Enantioselective hydrogenation of hydroxyphenyl styrenes5
• Samarium diiodide-mediated cyclization for synthesis of substituted benzannulated cyclooctanol derivatives6
• Suzuki-Miyaura cross-coupling for synthesis of C-6-substituted uridine phosphonates7

Description (简体中文)

Other Notes
含有不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reactant involved in:
• Halogenation of alkynes for preparation of enol esters1
• Liebeskind-Srogl cross-coupling2
• Homocoupling of arylboronic acids for synthesis of biaryls3
• Iterative cross-coupling of boronate building blocks4
• Enantioselective hydrogenation of hydroxyphenyl styrenes5
• Samarium diiodide-mediated cyclization for synthesis of substituted benzannulated cyclooctanol derivatives6
• Suzuki-Miyaura cross-coupling for synthesis of C-6-substituted uridine phosphonates7