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E-PHENYLETHENYLBORONIC ACID

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E-PHENYLETHENYLBORONIC ACID Basic information

Product Name:
E-PHENYLETHENYLBORONIC ACID
Synonyms:
  • trans-^b-Styrylboronic acid
  • trans-beta-Styrylboronic acid
  • STYRYLBORONIC ACID
  • RARECHEM AH PB 0201
  • TRANS-BETA-STYRENEBORONIC ACID
  • TRANS-B-STYRENEBORONIC ACID
  • TRANS-PHENYLETHENYLBORONIC ACID
  • TRANS-PHENYLVINYLBORONIC ACID
CAS:
6783-05-7
MF:
C8H9BO2
MW:
147.97
Product Categories:
  • Boronic Acids
  • blocks
  • BoronicAcids
  • Alkenyl Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Alkenyl
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Organometallic Reagents
Mol File:
6783-05-7.mol
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E-PHENYLETHENYLBORONIC ACID Chemical Properties

Melting point:
146-156 °C(lit.)
Boiling point:
315.9±35.0 °C(Predicted)
Density 
1.130±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
Powder and/or Chunks
pka
9.38±0.43(Predicted)
color 
Light yellow to beige
CAS DataBase Reference
6783-05-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29310099

MSDS

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E-PHENYLETHENYLBORONIC ACID Usage And Synthesis

Chemical Properties

Brown granular powder

Uses

trans-beta-Styrylboronic acid as reagent is used for palladium (Pd)-catalyzed Suzuki-Miyaura coupling reactions, diastereoselective synthesis via Pd-catalyzed Heck-Suzuki cascade reaction and rhodium (Rh)-catalyzed intramolecular amination of aryl azides. It is also used as reagent in preparation of optically active unsaturated amino acids by diastereoselective Petasis borono-Mannich reaction and amino alcohol dienes via Petasis 3-component reaction using Ru-catalyzed ring-closing metathesis and isomerization.

Uses

Reagent used for

  • Palladium (Pd)-catalyzed Suzuki-Miyaura coupling reactions
  • Rhodium (Rh)-catalyzed intramolecular amination of aryl azides
  • Diastereoselective synthesis via Pd-catalyzed Heck-Suzuki cascade reaction
  • Copper (Cu)-mediated cyanation
  • Rhodium (Rh)-catalyzed asymmetric addition
  • Diastereoselective synthesis via iridium (Ir)-catalyzed addition
  • Palladium (Pd)-catalyzed cascade cyclization

Reagent used in Preparation of
  • Optically active unsaturated amino acids by diastereoselective Petasis borono-Mannich reaction
  • Amino alcohol dienes via Petasis 3-component reaction using Ru-catalyzed ring-closing metathesis and isomerization

Uses

E-Phenylethenylboronic acid is a reagent used for• ;Palladium (Pd)-catalyzed Suzuki-Miyaura coupling reactions
1 Rhodium (Rh)-catalyzed intramolecular amination of aryl azides
2 Diastereoselective synthesis via Pd-catalyzed Heck-Suzuki cascade reaction
3 Copper (Cu)-mediated cyanation
4 Rhodium (Rh)-catalyzed asymmetric addition
5 Diastereoselective synthesis via iridium (Ir)-catalyzed addition
6 Palladium (Pd)-catalyzed cascade cyclization
7 Reagent used in Preparation of • ;Optically active unsaturated amino acids by diastereoselective Petasis borono-Mannich reactio

E-PHENYLETHENYLBORONIC ACID Preparation Products And Raw materials

Raw materials

E-PHENYLETHENYLBORONIC ACIDSupplier

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