missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Benzenoids
  6. Benzene and substituted derivatives
  7. Styrenes
  8. trans-beta-Styrylboronic acid, 97%

trans-beta-Styrylboronic acid, 97%

Product Code. 15429987
Change view
Click to view available options
Quantity:
1 g
5 g
Unit Size:
1g
5g
2 product options available for selection
Product selection table with 2 available options. Use arrow keys to navigate and Enter or Space to select.
Product Code. Quantity unitSize
15429987 1 g 1g
15439987 5 g 5g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 2 options available.
2 options
This item is not returnable. View return policy
Product Code. 15429987 Supplier Thermo Scientific Alfa Aesar Supplier No. H53227.03
Request Bulk or Custom Format

Please to purchase this item. Need a web account? Register with us today!

This item is not returnable. View return policy

Description

CAS: 6783-05-7 | C8H9BO2 | 147.97 g/mol

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.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 6783-05-7
MDL Number MFCD00963621

Specifications

Melting Point 98°C to 100°C
Molecular Formula C11H10N4O4
Quantity 1 g
Synonym carbadox, unii-m2x04r2e2y, getroxel, mecadox, dsstox_cid_23913, dsstox_rid_80088, dsstox_gsid_43913, fortigro, karbadox czech, methyl n-e-1-hydroxy-4-oxidoquinoxalin-4-ium-2-ylidene methyl iminocarbamate
InChI Key BPMVRAQIQQEBLN-UHFFFAOYSA-N
SMILES COC(=O)N=NC=C1C=[N+](C2=CC=CC=C2N1O)[O-]
IUPAC Name methyl N-[(E)-(1-hydroxy-4-oxidoquinoxalin-4-ium-2-ylidene)methyl]iminocarbamate
Molecular Weight (g/mol) 262.23
PubChem CID 5353472
Formula Weight 147.97
Percent Purity 97%
Chemical Name or Material trans-beta-Styrylboronic acid
Show More Show Less

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.