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2’-(Acetylthio)ethyl 2,3,4,6-Tetra-O-acetyl--D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34044-34-3

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34044-34-3 Usage

Chemical Properties

Clear Colourless Oil

Check Digit Verification of cas no

The CAS Registry Mumber 34044-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,4 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34044-34:
(7*3)+(6*4)+(5*0)+(4*4)+(3*4)+(2*3)+(1*4)=83
83 % 10 = 3
So 34044-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O11S/c1-9(19)25-8-14-15(26-10(2)20)16(27-11(3)21)17(28-12(4)22)18(29-14)24-6-7-30-13(5)23/h14-18H,6-8H2,1-5H3/t14?,15-,16+,17+,18-/m1/s1

34044-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(2-acetylsulfanylethoxy)oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 2-Mercaptoethyl |A-D-Glucopyranoside Pentaacetate

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:34044-34-3 SDS

34044-34-3Downstream Products

34044-34-3Relevant academic research and scientific papers

Conversion of 2-(trimethylsilyl)ethyl sulfides into thioesters

Grundberg, Hans,Andergran, Magnus,Nilsson, Ulf J.

, p. 1811 - 1814 (2007/10/03)

Treatment of 2-(trimethylsilyl)ethyl sulfides with a carboxylic acid chloride and AgBF4 in CH2Cl2 furnishes the corresponding thioesters in high yields and purities. The conversion of 2-(trimethylsilyl)ethyl sulfides into synthetically versatile thioesters allows such sulfides to be used as sulfhydryl protective groups, since such sulfides are easily prepared and are stable towards many reaction conditions encountered in organic syntheses.

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