Substance
ID:344019
Names and Identifiers
IUPAC name
(1-phenylethenyl)boronic acid
IUPAC Traditional name
1-phenylethenylboronic acid
Synonyms
1-Phenylvinylboronic acid(1-Phenylethenyl)boronic acidStyrene α-boronic acid1-苯基乙烯基硼酸α-Methylene-α-tolueneboronic acidα-苯基乙烯基硼酸α-Phenyl vinylboronic acid
Properties
Safety Information
Storage Temperature
2-8°C
German water hazard class
3
MSDS Link
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Product Information
Purity
95%
Linear Formula
C6H5C=CH2B(OH)2
Physical Property
Melting Point
125 °C (dec.)(lit.)
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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