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C-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL) THIOFORMAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358738-47-3

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358738-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358738-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,7,3 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 358738-47:
(8*3)+(7*5)+(6*8)+(5*7)+(4*3)+(3*8)+(2*4)+(1*7)=193
193 % 10 = 3
So 358738-47-3 is a valid CAS Registry Number.

358738-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name C-(2,3,4,6-TETRA-O-ACETYL-β-D-GALACTOPYRANOSYL) THIOFORMAMIDE

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:358738-47-3 SDS

358738-47-3Downstream Products

358738-47-3Relevant academic research and scientific papers

Preparation of 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles from C-(β-D-glycopyranosyl)thioformamides

Osz,Czifrák,Deim,Szilágyi,Bényei,Somsák

, p. 5429 - 5434 (2001)

Acylated C-glycopyranosyl thioformamides of D-gluco, D-galacto, and D-xylo configuration were obtained by treating the corresponding glycosyl cyanides with hydrogen sulfide in the presence of triethylamine. The thioformamides gave 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles in reactions with potassium bromate and sodium dithionite in dichloromethane-water biphasic solvent mixture. Deprotected derivatives were prepared by Zemple?n deacylation.

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