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19779-76-1

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19779-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19779-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,7 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19779-76:
(7*1)+(6*9)+(5*7)+(4*7)+(3*9)+(2*7)+(1*6)=171
171 % 10 = 1
So 19779-76-1 is a valid CAS Registry Number.

19779-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-Na-methyl-Nb-benzyltriptophan methyl ester

1.2 Other means of identification

Product number -
Other names N-Benzyl-1-methyl-dl-tryptophan-methylester

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:19779-76-1 SDS

19779-76-1Downstream Products

19779-76-1Relevant articles and documents

Selenium Dioxide Oxidations in the Indole Area. Synthesis of β-Carboline Alkaloids

Cain, M.,Campos, O.,Guzman, F.,Cook, J.M.

, p. 907 - 913 (2007/10/02)

A number of different piperidoindole systems have been subjected to oxidation with selenium dioxide.The bonding between the indole and piperidine unit has been varied to provide different systems, the oxidation of which has led to formation of either 2-acyl- or 3-acylindoles or fully aromatic β-carbolines, depending on the substrate chosen.The pattern of reactivity observed was in complete agreement with the ene mechanism proposed for selenium dioxide oxidations, and this can be employed to predict the regiochemistry of the oxidation.Use of this technology has resulted in a two-step synthesis of the indole alkaloid canthin-6-one (30a).

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