Thermo Scientific Chemicals

trans-beta-Styrylboronic acid, 97%, Thermo Scientific Chemicals

製品番号(カタログ番号): H53227.06
5 g, Each
Thermo Scientific Chemicals

trans-beta-Styrylboronic acid, 97%, Thermo Scientific Chemicals

製品番号(カタログ番号): H53227.06
5 g, Each
数量
製品番号(カタログ番号): H53227.06
または、製品番号H53227-06

化学物質識別子

CAS
6783-05-7
IUPAC Name
[(1E)-2-phenylethenyl]boronic acid
Molecular Formula
C8H9BO2
InChI Key
VKIJXFIYBAYHOE-VOTSOKGWSA-N
SMILES
OB(O)C=CC1=CC=CC=C1
Assay (HPLC)
96.0% min

概要

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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and heat.
RUO – Research Use Only

ドキュメントおよびダウンロード

証明書

    よくあるご質問(FAQ)

    引用および参考文献

    Search citations by name, author, journal title or abstract text