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trans-2-Phenylvinylboronic acid_Molecular_structure_CAS_6783-05-7)
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trans-2-Phenylvinylboronic acid

Catalog No. 473790 Name Sigma Aldrich
CAS Number 6783-05-7 Website http://www.sigmaaldrich.com
M. F. C8H9BO2 Telephone 1-800-521-8956
M. W. 147.96686 Fax
Purity 97% Email
Storage Chembase ID: 74813

SYNONYMS

Title
反式-2-苯基乙烯基硼酸
IUPAC name
[(E)-2-phenylethenyl]boronic acid
IUPAC Traditional name
(E)-2-phenylethenylboronic acid
Synonyms
trans-(2-Phenylethenyl)boronic acid
(E)-Phenylethenylboronic acid
(E)-2-phenyl-Etheneboronic acid
(E)-Styreneboronic acid
(E)-Styrylboronic acid
trans-Phenylvinyl boronic acid

DATABASE IDS

PubChem SID 24870932
MDL Number MFCD00963621
CAS Number 6783-05-7

PROPERTIES

Linear Formula C6H5CH=CHB(OH)2
Purity 97%
Melting Point 146-156 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
25 g in poly bottle
5 g in glass bottle
Application
Reagent used for
• Palladium (Pd)-catalyzed Suzuki-Miyaura coupling reactions1
• Rhodium (Rh)-catalyzed intramolecular amination of aryl azides2
• Diastereoselective synthesis via Pd-catalyzed Heck-Suzuki cascade reaction3
• Copper (Cu)-mediated cyanation4
• Rhodium (Rh)-catalyzed asymmetric addition5
• Diastereoselective synthesis via iridium (Ir)-catalyzed addition6
• Palladium (Pd)-catalyzed cascade cyclization7 Reagent used in Preparation of
• Optically active unsaturated amino acids by diastereoselective Petasis borono-Mannich reaction8
• Amino alcohol dienes via Petasis 3-component reaction using Ru-catalyzed ring-closing metathesis and isomerization9
Description (简体中文)
Other Notes
含有不定量的酸酐
包装
25 g in poly bottle
5 g in glass bottle
Application
Reagent used for
• Palladium (Pd)-catalyzed Suzuki-Miyaura coupling reactions1
• Rhodium (Rh)-catalyzed intramolecular amination of aryl azides2
• Diastereoselective synthesis via Pd-catalyzed Heck-Suzuki cascade reaction3
• Copper (Cu)-mediated cyanation4
• Rhodium (Rh)-catalyzed asymmetric addition5
• Diastereoselective synthesis via iridium (Ir)-catalyzed addition6
• Palladium (Pd)-catalyzed cascade cyclization7 Reagent used in Preparation of
• Optically active unsaturated amino acids by diastereoselective Petasis borono-Mannich reaction8
• Amino alcohol dienes via Petasis 3-component reaction using Ru-catalyzed ring-closing metathesis and isomerization9

REFERENCES