E-PHENYLETHENYLBORONIC ACID
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
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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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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