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876-37-9

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876-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876-37-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 876-37:
(5*8)+(4*7)+(3*6)+(2*3)+(1*7)=99
99 % 10 = 9
So 876-37-9 is a valid CAS Registry Number.

876-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(8R,9S,10S,13S,14S)-17-ethynyl-17-hydroxy-13-methyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-10-yl]methyl acetate

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:876-37-9 SDS

876-37-9Upstream product

876-37-9Downstream Products

876-37-9Relevant articles and documents

Stereospecific cyclodehydration of 1,4-sulfanylalcohols to thiolanes: mechanistic insights

Filippi, Jean-Jacques,Du?ach, Elisabet,Fernandez, Xavier,Meierhenrich, Uwe J.

experimental part, p. 9999 - 10003 (2009/04/03)

A series of thiolanes were prepared by cyclodehydration of sulfanylalcohols in the presence of catalytic amounts of p-toluenesulfonic acid or by using K10 clay. The sulfur heterocycles were synthesised in good to excellent yields using either a conventional Dean-Stark method or microwave irradiation under solvent-free conditions. The reaction could be performed regio- and stereoselectively and its mechanism was investigated by means of enantio- and diastereomerically enriched substrates. In contrast to previous studies, our results are consistent with an intramolecular SN2-type mechanism as a general pathway.

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