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1H-Indole-1-carboxylic acid, 3-[(4-bromophenyl)methyl]-2,3-dihydro-2-oxo-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923568-92-7

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923568-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923568-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,5,6 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 923568-92:
(8*9)+(7*2)+(6*3)+(5*5)+(4*6)+(3*8)+(2*9)+(1*2)=197
197 % 10 = 7
So 923568-92-7 is a valid CAS Registry Number.

923568-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-t-butoxycarbonyl-3-(4-bromobenzyl)-2-oxindole

1.2 Other means of identification

Product number -
Other names 3-(4-Bromo-benzyl)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester

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:923568-92-7 SDS

923568-92-7Relevant academic research and scientific papers

Synthesis, Characterization, and Reactivity of a Hypervalent-Iodine-Based Nitrooxylating Reagent

Calvo, Roxan,Katayev, Dmitry,Le Tellier, Antoine,Nater, Darryl,Nauser, Thomas,Rombach, David

, p. 17162 - 17168 (2020/07/31)

Herein, the synthesis and characterization of a hypervalent-iodine-based reagent that enables a direct and selective nitrooxylation of enolizable C?H bonds to access a broad array of organic nitrate esters is reported. This compound is bench stable, easy-

Lewis acid-catalyzed enantioselective hydroxylation reactions of oxindoles and β-keto esters using DBFOX ligand

Ishimaru, Takehisa,Shibata, Norio,Nagai, Jun,Nakamura, Shuichi,Toru, Takeshi,Kanemasa, Shuji

, p. 16488 - 16489 (2007/10/03)

The first catalytic enantioselective hydroxylation reaction of both 3-aryl and 3-alkyl-2-oxindoles using the DBFOX-Zn(II) complex, leading to pharmaceutically important chiral 3-hydroxy-2-oxindoles was described. The structure of oxidant was found to play

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