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2,5-Anhydro-D-allonothioamide 3,4,6-Tribenzoate is a chemical compound that serves as an intermediate in the synthesis of Tiazofurin (T437200), a potential therapeutic agent for the treatment of cancer. It is characterized by its unique molecular structure and plays a crucial role in the development of pharmaceuticals targeting cancer cells.

57944-10-2

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57944-10-2 Usage

Uses

Used in Pharmaceutical Industry:
2,5-Anhydro-D-allonothioamide 3,4,6-Tribenzoate is used as a key intermediate in the synthesis of Tiazofurin (T437200) for its potential therapeutic application in cancer treatment. 2,5-Anhydro-D-allonothioaMide 3,4,6-Tribenzoate contributes to the development of new drugs that can target and combat cancer cells effectively.
Used in Cancer Treatment:
2,5-Anhydro-D-allonothioamide 3,4,6-Tribenzoate is used as a precursor in the production of Tiazofurin (T437200), which is being explored for its potential as an anticancer agent. 2,5-Anhydro-D-allonothioaMide 3,4,6-Tribenzoate plays a significant role in the development of therapeutic strategies aimed at treating various types of cancer by enhancing the effectiveness of cancer treatments and improving patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 57944-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,4 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57944-10:
(7*5)+(6*7)+(5*9)+(4*4)+(3*4)+(2*1)+(1*0)=152
152 % 10 = 2
So 57944-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H23NO7S/c28-24(36)23-22(35-27(31)19-14-8-3-9-15-19)21(34-26(30)18-12-6-2-7-13-18)20(33-23)16-32-25(29)17-10-4-1-5-11-17/h1-15,20-23H,16H2,(H2,28,36)

57944-10-2SDS

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 (3,4-dibenzoyloxy-5-carbamothioyloxolan-2-yl)methyl benzoate

1.2 Other means of identification

Product number -
Other names 2,5-anhydro-3,4,6-tri-O-benzoyl-D-allonthioamide

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:57944-10-2 SDS

57944-10-2Relevant academic research and scientific papers

COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USE THEREOF AS INHIBITORS OF RAN GTPASE

-

, (2019/04/09)

Compounds of general formula IA, IB and IC outlined below, including pharmaceutically acceptable salts, solvates and hydrates thereof. Such compounds and pharmaceutical compositions comprising them may be used in medical conditions involving Ran GTPase.

A modified synthesis of tiazofurin

Ramasamy, Kanda S.,Averett, Devron

, p. 2425 - 2431 (2007/10/03)

An improved synthesis of tiazofurin is described from 1-O-acetyl-2,3,5- tri-O-benzoyl-β-D-ribofuranose.

Synthesis and structure-activity relationships of a series of novel thiazoles as inhibitors of aminoacyl-tRNA synthetases

Yu, Xiang Y.,Hill, Jason M.,Yu, Guixue,Wang, Weiheng,Kluge, Arthur F.,Wendler, Phil,Gallant, Paul

, p. 375 - 380 (2007/10/03)

A series of novel aminoacyl adenylate mimics has been prepared and evaluated for their inhibitory activity against aminoacyl-tRNA synthetases. Several of these thiazole derivatives displayed potent and selective enzyme activity against both Gram-positive and Gram-negative bacteria.

Procedures for obtaining ribo-C-nucleosides

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, (2008/06/13)

Novel procedures for obtaining ribo-C-nucleosides, including especially 2-β-D-ribofuranosylthiazole-4-carboxylamide (tiazofirin) and 2-β-D-ribofuranosylselenazole-4-carboxylamide (sylenazofurin) and synthesis intermediates thereof. The novel procedures in

Process for the production of 2-β-D-ribofuranosylthiazole-4-carboxamide

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, (2008/06/13)

An improved multi-step process for the production of 2-β-D-ribofuranosylthiazole-4-carboxamide.

Synthesis and antiviral activity of certain thiazole C nucleosides

Srivastava,Pickering,Allen,Streeter,Campbell,Witkowski,Sidwell,Robins

, p. 256 - 262 (2007/10/08)

A general reaction of glycosyl cyanides with liquid hydrogen sulfide in the presence of 4 dimethylaminopyridine to provide the corresponding glycosylthiocarboxamides is described. These glycosylthiocarboxamides were utilized as the precursors for the synt

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