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102029-58-3

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102029-58-3 Usage

General Description

3-O-ACETYL-6-O -BENZOYL-5-O-(METHYLSULFONYL)-1,2-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSE is a complex compound with various functional groups. It consists of an isopropylidene group, a glucopyranose ring, and acetyl, benzoyl, and methylsulfonyl substituents. 3-O-ACETYL-6-O -BENZOYL-5-O-(METHYLSULFONYL)-1,2-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSE is often used in the synthesis of other organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a versatile building block for creating new molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 102029-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,2 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102029-58:
(8*1)+(7*0)+(6*2)+(5*0)+(4*2)+(3*9)+(2*5)+(1*8)=73
73 % 10 = 3
So 102029-58-3 is a valid CAS Registry Number.

102029-58-3SDS

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)-2-[(3aR,5S,6S,6aR)-6-acetyloxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-methylsulfonyloxyethyl] benzoate

1.2 Other means of identification

Product number -
Other names 3-O-Acetyl-6-O-benzoyl-5-O-(methylsulfonyl)-1,2-O-isopropylidene-|A-D-glucofuranose

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:102029-58-3 SDS

102029-58-3Relevant articles and documents

Synthesis and Evaluation of 1,5-Dithia- d -laminaribiose, Triose, and Tetraose as Truncated β-(1→3)-Glucan Mimetics

Liao, Xiaoxiao,Větvi?ka, Václav,Crich, David

, p. 14894 - 14904 (2018)

The preparation and characterization of a series of di-, tri-, and tetrasaccharide analogues of β-(1→3)-glucans is described in which each pyranoside ring is replaced by a 5-thiopyranosyl ring and each glycosidic oxygen by a thioether. These oligomeric 1,

Synthesis of Per-O-alkylated 5-Thio-D-glucono-1,5-lactones and Transannular Participation of the Ring Sulphur Atom of 5-Thio-D-glucose Derivatives on Solvolysis under Acidic Conditions

Yuasa, Hideya,Tamura, Jun-ichi,Hashimoto, Hironobu

, p. 2763 - 2769 (2007/10/02)

Per-O-alkylated 5-thio-D-glucono-1,5-lactones (33)-(35) were synthesized via acetolysis or hydrolysis of the corresponding methyl glycosides (21)-(23).Transannular participation of the sulphur atom on acid methanolysis of 3,6-di-O-acetyl-5-S-acetyl-1,2-O-

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