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5-Pyridin-2-yl-4,5-dihydro-1,3,4-thiadiazole-2-thiol is a chemical compound with the molecular formula C6H6N2S3. It is a heterocyclic compound, featuring a pyridine ring and a 1,3,4-thiadiazole ring connected through a sulfur atom. 5-PYRIDIN-2-YL-4,5-DIHYDRO-1,3,4-THIADIAZOLE-2-THIOL is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can act as a building block for the development of new molecules with specific biological activities. The compound's properties, such as its solubility and stability, can be influenced by the presence of different functional groups and substituents on the pyridine and thiadiazole rings. Research into this class of compounds is ongoing to explore their potential uses in various industries.

5757-43-7

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5757-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5757-43-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5757-43:
(6*5)+(5*7)+(4*5)+(3*7)+(2*4)+(1*3)=117
117 % 10 = 7
So 5757-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3S2/c11-7-10-9-6(12-7)5-3-1-2-4-8-5/h1-4,6,9H,(H,10,11)

5757-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pyridin-2-yl-1,3,4-thiadiazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 5-pyridin-2-yl-[1,3,4]thiadiazolidine-2-thione

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:5757-43-7 SDS

5757-43-7Downstream Products

5757-43-7Relevant academic research and scientific papers

2-Arylidene Hydrazinecarbodithioates as Potent, Selective Inhibitors of Cystathionine γ-Lyase (CSE)

Bhattacharjee, Abir,Sinha, Antara,Ratia, Kiira,Yin, Liang,Delgado-Rivera, Loruhama,Petukhov, Pavel A,Thatcher, Gregory R. J.,Wardrop, Duncan J.

, p. 1241 - 1245 (2017/12/26)

Hydrogen sulfide is produced from l-cysteine by the action of both cystathionine γ-lyase (CSE) and cystathionine β-synthase (CBS) and increasingly has been found to play a profound regulatory role in a range of physiological processes. Mounting evidence suggests that upregulation of hydrogen sulfide biosynthesis occurs in several disease states, including rheumatoid arthritis, hypertension, ischemic injury, and sleep-disordered breathing. In addition to being critical tools in our understanding of hydrogen sulfide biology, inhibitors of CSE hold therapeutic potential for the treatment of diseases in which increased levels of this gasotransmitter play a role. We describe the discovery and development of a novel series of potent CSE inhibitors that show increased activity over the benchmark inhibitor and, importantly, display high selectivity for CSE versus CBS.

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