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19206-51-0

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19206-51-0 Usage

Uses

2-(2-Hydroxyethyl)benzeneboronic acid hemiester is used as an organic chemical synthesis intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 19206-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,0 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19206-51:
(7*1)+(6*9)+(5*2)+(4*0)+(3*6)+(2*5)+(1*1)=100
100 % 10 = 0
So 19206-51-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BO2/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-4,10H,5-6H2

19206-51-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H52672)  2-(2-Hydroxyethyl)benzeneboronic acid hemiester, 95%   

  • 19206-51-0

  • 250mg

  • 2470.0CNY

  • Detail

19206-51-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3,4-dihydro-2,1-benzoxaborinine

1.2 Other means of identification

Product number -
Other names OR3329

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19206-51-0 SDS

19206-51-0Relevant articles and documents

An Efficient Benzoxaborole One-Pot Synthesis by SiliaCat DPP-Pd Heterogeneous Catalysis using Diboronic Acid

Kunihiro, Kana,Dumais, Laurence,Lafitte, Guillaume,Varvier, Emeric,Tomas, Lo?c,Harris, Craig S.

, p. 2757 - 2761 (2018)

Organoboron compounds are valuable molecules of increasing interest in organic synthesis, catalysis, biology and medicine. Among them, benzoxaboroles emerged as promising building blocks for numerous research programs. In this letter, we communicate the development of new conditions for the one-pot benzoxaborole synthesis by SiliaCat DPP?Pd catalysis using diboronic acid as the boron source. This low cost and sustainable strategy permitted the preparation of a useful range of benzoxaborole building blocks. Finally, the transformation was extended to a continuous flow process using our Vapourtec system. (Figure presented.).

A convenient one-pot synthesis of boroxoles from diboronic acid

Lafitte, Guillaume,Kunihiro, Kana,Bonneaud, Céline,Dréan, Bénédicte,Gaigne, Frédéric,Parnet, Véronique,Pierre, Romain,Raffin, Catherine,Vatinel, Rodolphe,Fournier, Jean-Fran?ois,Musicki, Branislav,Ouvry, Gilles,Bouix-Peter, Claire,Tomas, Loic,Harris, Craig S.

supporting information, p. 3757 - 3759 (2017/09/12)

The preparation of the boroxole motif traditionally relies on a 3-step process and the use of n-butyl lithium that can limit substrate scope. Herein during our exploration toward novel RORγ inhibitors, we identified a convenient one-pot preparation of the motif in good yields with good substrate scope.

BORON-CONTAINING SMALL MOLECULES AS ANTI-PROTOZOAL AGENT

-

Page/Page column 78, (2011/10/10)

This invention provides, among other things, novel compounds useful for treating protozoal infections, pharmaceutical compositions containing such compounds, as well as combinations of these compounds with at least one additional therapeutically effective agent. The compounds are of the formula, wherein Y' is a halogen, Y is halosubstituted alkyl, or a salt thereof.

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