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2,5-anhydro-1-O-(4-tolylsulfonyl)mannitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84447-04-1

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84447-04-1 Usage

Molecular Weight

380.45 g/mol; the compound's relative molecular mass based on the atomic weights of its constituent atoms.

Derivation

Mannitol-based; the compound is derived from mannitol, a naturally occurring sugar alcohol.

Modification

Tosyl group; the compound has been modified with a tosyl group, which increases its reactivity.

Utility

Organic synthesis; the compound is useful as a building block in the synthesis of other organic molecules.

Pharmaceutical potential

Antiproliferative and antiviral properties; the compound has been studied for its potential as a pharmaceutical compound with possible applications in the treatment of diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 84447-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84447-04:
(7*8)+(6*4)+(5*4)+(4*4)+(3*7)+(2*0)+(1*4)=141
141 % 10 = 1
So 84447-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O7S/c1-8-2-4-9(5-3-8)21(17,18)19-7-11-13(16)12(15)10(6-14)20-11/h2-5,10-16H,6-7H2,1H3/t10-,11-,12-,13-/m1/s1

84447-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-anhydro-1-O-(p-tolylsulfonyl)-D-mannitol

1.2 Other means of identification

Product number -
Other names 2,5-anhydro-1-O-tosyl-D-mannitol

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:84447-04-1 SDS

84447-04-1Relevant academic research and scientific papers

A simple O-sulfated thiohydroximate molecule to be the first micromolar range myrosinase inhibitor

Cerniauskaite, Deimante,Gallienne, Estelle,Karciauskaite, Henreta,Farinha, Andrea S.F.,Rousseau, Jolanta,Armand, Sylvie,Tatibou?t, Arnaud,Sackus, Algirdas,Rollin, Patrick

body text, p. 3302 - 3305 (2009/08/09)

New non-hydrolyzable analogues of glucosinolates have been prepared. Myrosinase inhibition was observed with modified aglycon moieties, even bulky phenothiazine analogue 6 gave reasonable inhibition. The simplest structure 8 derived from dimethylaminoethanethiol has shown to be the most potent inhibitor with an IC50 of 3.32 μM.

Ethambutol-sugar hybrids as potential inhibitors of mycobacterial cell-wall biosynthesis

Reynolds, Robert C.,Bansal, Namita,Rose, Jerry,Friedrich, Joyce,Suling, William J.,Maddry, Joseph A.

, p. 164 - 179 (2007/10/03)

Ethambutol is an established front-line agent for the treatment of tuberculosis, and is also active against Mycobacterium avium infection. However, this agent exhibits toxicity, and is considered to have low potency. The action of ethambutol on the mycoba

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