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thiobenzoic acid S-(2-morpholin-4-yl-2-oxo-ethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

380451-93-4

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380451-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380451-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,4,5 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 380451-93:
(8*3)+(7*8)+(6*0)+(5*4)+(4*5)+(3*1)+(2*9)+(1*3)=144
144 % 10 = 4
So 380451-93-4 is a valid CAS Registry Number.

380451-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(2-morpholino-2-oxoethyl) benzothioate

1.2 Other means of identification

Product number -
Other names -

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:380451-93-4 SDS

380451-93-4Relevant academic research and scientific papers

Copper-Mediated, Palladium-Catalyzed Coupling of Thiol Esters with Aliphatic Organoboron Reagents

Yu, Ying,Liebeskind, Lanny S.

, p. 3554 - 3557 (2007/10/03)

Thiol esters and B-alkyl-9-BBN derivatives couple in the presence of a copper(I) carboxylate mediator and a palladium catalyst. In contrast to copper-mediated, palladium-catalyzed cross-couplings of thioorganics with boronic acids, the current coupling reaction of 9-BBN derivatives is facilitated by the addition of a base such as Cs2CO3. Under optimized conditions, a variety of thiol esters react with different B-alkyl-9-BBN derivatives giving ketones in moderate to excellent yields.

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