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73166-21-9

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73166-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73166-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,6 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73166-21:
(7*7)+(6*3)+(5*1)+(4*6)+(3*6)+(2*2)+(1*1)=119
119 % 10 = 9
So 73166-21-9 is a valid CAS Registry Number.

73166-21-9SDS

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 2,4,5,6-Tetrahydro-8-methyl-1H-pyrazino(3,2,1-jk)carbazole monohydrochloride

1.2 Other means of identification

Product number -
Other names 1H-Pyrazino(3,2,1-jk)carbazole,2,4,5,6-tetrahydro-8-methyl-,monohydrochloride

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:73166-21-9 SDS

73166-21-9Downstream Products

73166-21-9Relevant articles and documents

First Preparative Enantiomer Resolution of Pirlindole, a Potent Antidepressant Drug

De Tullio, Pascal,Felikidis, Apostolos,Pirotte, Bernard,Liegeois, Jean-Francois,Stachow, Monique,Delarge, Jacques,Ceccato, Attilio,Hubert, Philippe,Crommen, Jacques,Geczy, Joseph

, p. 539 - 547 (2007/10/03)

Pirlindole is an antidepressant drug. It acts principally as reversible inhibitor of monoamine oxidase-A (RIMA) and appears relatively potent in comparison with reference drugs. Pirlindole possesses stereogenic center but is generally used as racemate. In this work, the first preparative resolution of its enantiomeric couple is described. Whereas selective crystallization of salts of chiral acid failed, two asymmetric synthetic pathways were also examined; however, without success. Finally separation and isolation of enantiomers of pirlindole was completed by using the derivatization method coupled with preparative HPLC. Optical purity of each isomer was determined by chiral HPLC. The specific rotation of each antipode was also determined.

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