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763047-58-1

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763047-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 763047-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,3,0,4 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 763047-58:
(8*7)+(7*6)+(6*3)+(5*0)+(4*4)+(3*7)+(2*5)+(1*8)=171
171 % 10 = 1
So 763047-58-1 is a valid CAS Registry Number.

763047-58-1SDS

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 2,3-dihydroindole-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names L-indoline carboxylic acid

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:763047-58-1 SDS

763047-58-1Relevant articles and documents

Solvent-dependent effect by carbon dioxide on the photoreactions of (9-anthryl)alkylamines

Horiguchi, Masahiro,Ito, Yoshikatsu

, p. 12286 - 12293 (2008/09/16)

The effect of CO2 on a photoreaction was first studied systematically by using (9-anthryl)alkylamines (APA, AEA, and AMA) as the starting compound. From close scrutiny of the results, the CO2 effect was clearly observed and was well rationalized by the previously reported novel solvent dependence of the amine-CO2 reversible reactions. For instance, the yield of the dimer (h-t from APA or AEA, h-t+h-h from AMA) obtained in MeOH or DMSO was higher under CO2 than under argon and this was ascribed to formation of either ammonium bicarbonate/carbonate in MeOH or carbamic acid in DMSO, which will prevent the nitrogen lone pair from being involved in electron-transfer reactions. In fact, the electron-transfer side reactions producing 1-3 in DMSO were strongly inhibited under CO2. Also, due to formation of noncovalent linkage between the ammonium cation and the carbamate anion in 2-PrOH, the proportion of h-h relative to h-t produced from AMA in 2-PrOH was increased by carrying out the reaction under CO2.

Process for the preparation of an indoline carboxylic acid

-

, (2008/06/13)

The invention relates to a novel process for the preparation of the optically pure 2S- or 2R-indolinecarboxylic acid of the formula STR1 and salts thereof. The process comprises forming the heterocyclic 5-membered ring in formula I from an open chain prec

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