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20939-17-7

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20939-17-7 Usage

Type of Compound

Small molecule inhibitor

Target Enzyme

Glycogen synthase kinase-3 (GSK-3)

Enzyme Function

Regulation of cellular processes such as metabolism, gene expression, and apoptosis

Potential Therapeutic Applications

Neurodegenerative diseases (e.g., Alzheimer's, Parkinson's) and various forms of cancer

Mechanism of Action

Inhibition of GSK-3 and modulation of various signaling pathways

Current Status

Promising candidate for further research and development as a potential therapeutic agent

Preclinical Studies

Shown promise in treating neurodegenerative diseases and cancer

Structure

Contains a thiadiazolidine ring with two dithione groups at positions 3 and 5

Check Digit Verification of cas no

The CAS Registry Mumber 20939-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,3 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20939-17:
(7*2)+(6*0)+(5*9)+(4*3)+(3*9)+(2*1)+(1*7)=107
107 % 10 = 7
So 20939-17-7 is a valid CAS Registry Number.
InChI:InChI=1/CHNOS/c2-1-3-4/h4H

20939-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-thiadiazolidine-3,5-dithione

1.2 Other means of identification

Product number -
Other names 1,2,4-Thiadiazole-3,5-dithiol

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:20939-17-7 SDS

20939-17-7Relevant articles and documents

Synthesis of 2-amino-5(6)-(4-aminophenyl)benzimidazole derivatives: II. Reaction of 2-nitro-4-thiocyanatoaniline with 4-nitrochlorobenzene

Pilyugin,Sapozhnikov,Shitov

, p. 979 - 984 (2007/10/03)

The reaction of 2-nitro-4-thiocyanatoaniline with 4-nitrochlorobenzene in aqueous alkaline medium in the presence of phase-transfer catalyst at 95-100°C was studied with a view to obtain 4-amino-3,4′- dinitrodiphenyl sulfide. Optimal conditions for the synthesis and isolation of the product were found.

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