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benzyl 2,3-anhydro-4-O-[(trifluoromethyl)sulfonyl]-alpha-D-lyxopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71204-46-1

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71204-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71204-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,0 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71204-46:
(7*7)+(6*1)+(5*2)+(4*0)+(3*4)+(2*4)+(1*6)=91
91 % 10 = 1
So 71204-46-1 is a valid CAS Registry Number.

71204-46-1SDS

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 benzyl 2,3-anhydro-4-O-(trifluoromethylsulfonyl)-α-D-lyxopyranoside

1.2 Other means of identification

Product number -
Other names benzyl 2,3-anhydro-4-triflyl-α-D-lyxopyranoside

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:71204-46-1 SDS

71204-46-1Relevant academic research and scientific papers

On the preparation of carbohydrate sulfates by displacement of trifluoromethanesulfonates

Hyatt,Little

, p. 215 - 217 (2007/10/02)

This paper reports on the preparation of carbohydrate sulfates by displacement of trifluoromethanesulfonates.

A Convenient Synthesis of 4-Amino-4-desoxy Sugars

Malik, Abdul,Roosz, Michael,Voelter, Wolfgang

, p. 559 - 561 (2007/10/02)

Displacement of the triflyl by the amino group in benzyl-2,3-anhydro-4-triflyl-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-amino-4-desoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced by

Synthesis of Sugar Nitrates by Nucloephilic Substitution

Afza, Nighat,Malik, Abdul,Latif, Farzana,Voelter, Wolfgang

, p. 1929 - 1934 (2007/10/02)

A rapid high-yielding synthesis of sugar mono- and dinitrates has been achieved via displacement of the trifluoromethylsulfonyloxy (triflate) by the nitrate group.This procedure is mild, convenient, and does not attack highly acid-labile groups.It also do

C-4-Triflate Displacement by Azide in 2,3-Anhydro Sugars; a New Way to 4-Amino-4-deoxy Sugars

Kimmich, Reinhard,Voelter, Wolfgang

, p. 1100 - 1104 (2007/10/02)

Displacement of the triflyl by the azido group in benzyl-2,3-anhydro-4-triflyl-α-D-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-azido-4-deoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced

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