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187343-15-3

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187343-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187343-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,3,4 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 187343-15:
(8*1)+(7*8)+(6*7)+(5*3)+(4*4)+(3*3)+(2*1)+(1*5)=153
153 % 10 = 3
So 187343-15-3 is a valid CAS Registry Number.

187343-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3:4,6-Di-O-benzylidene-2,5-dideoxy-2,5-imino-L-iditol

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:187343-15-3 SDS

187343-15-3Relevant articles and documents

Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors

Nasi, Ravindranath,Pinto, B. Mario

, p. 2305 - 2311 (2007/10/03)

The synthesis of new analogues of the naturally occurring glycosidase inhibitor, salacinol, and its ammonium analogue, ghavamiol is described. These analogues contain an additional hydroxymethyl group at C-1, which was intended to form additional polar co

Asymmetric Diels-Alder Cycloadditions with C2-Symmetrical Chiral Carbamoylnitroso Dienophiles

Defoin, Albert,Brouillard-Piochet, Agnes,Streith, Jacques

, p. 103 - 109 (2007/10/02)

The C2-symmetrical chiral pyrrolidines 2 and 3 are of opposite helicity.The corresponding N-acylnitroso dienophiles 6 and 7 react in good yield with cyclohexadiene, leading thereby with excellent diastereoisomeric excess to the expected Diels-A

A Short and Practical Synthesis of (2S,5S)-Bishydroxymethyl-(3R,4R)-bishydroxypyrrolidine

Shing, Tony K. M.

, p. 262 - 263 (2007/10/02)

D-Mannitol has been converted by five sequential reactions (benzylidenation, trifluoromethanesulphonation, hydrazinolysis, hydrogenolysis, and deacetalisation) into (2S,5S)-bishydroxymethyl-(3R,Ρ)-bishydroxypyrrolidine.

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