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3-O-[(4-methylphenyl)sulfonyl]hexopyranose is a complex organic chemical compound with the molecular formula C13H18O6S. It is a derivative of hexopyranose, a type of sugar molecule, with a 4-methylphenylsulfonyl group attached to the 3-O position. 3-O-[(4-methylphenyl)sulfonyl]hexopyranose is characterized by its unique structure, which features a hexopyranose ring with a sulfonyl group attached to the 4-methylphenyl moiety. It is an important intermediate in the synthesis of various biologically active compounds and pharmaceuticals, particularly those involving sugar-based molecules. The compound's properties, such as its solubility and reactivity, make it a valuable tool in organic synthesis and medicinal chemistry.

7702-25-2

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7702-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7702-25-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7702-25:
(6*7)+(5*7)+(4*0)+(3*2)+(2*2)+(1*5)=92
92 % 10 = 2
So 7702-25-2 is a valid CAS Registry Number.

7702-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,3,5-trihydroxy-6-(hydroxymethyl)oxan-4-yl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 3-O-Tolyl-p-sulfonyl-D-glucose

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:7702-25-2 SDS

7702-25-2Downstream Products

7702-25-2Relevant academic research and scientific papers

Extending the Scope of GTFR Glucosylation Reactions with Tosylated Substrates for Rare Sugars Synthesis

G?rl, Julian,Possiel, Christian,Sotriffer, Christoph,Seibel, Jürgen

, p. 2012 - 2015 (2017)

Functionalized rare sugars were synthesized with 2-, 3-, and 6-tosylated glucose derivatives as acceptor substrates by transglucosylation with sucrose and the glucansucrase GTFR from Streptococcus oralis. The 2- and 3-tosylated glucose derivatives yielded

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