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Ethyl 5-hydroxy-3-mercapto-1,2,4-triazine-6-carboxylate is a chemical compound characterized by its molecular formula C6H7N3O3S. It features a triazine ring with a hydroxyl group and a thiol group attached, along with an ethyl ester group and a carboxylate group. This versatile compound is widely recognized for its role as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. The presence of the thiol group makes it particularly suitable for the synthesis of thiazoline and thiazole derivatives, while its hydroxyl group suggests potential interactions with biological systems, highlighting its significance in medicinal chemistry research. Ethyl 5-hydroxy-3-mercapto-1,2,4-triazine-6-carboxylate holds promise for applications across various fields, including medicine, agriculture, and materials science.

51101-09-8

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  • Ethyl 5-oxo-3-thioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylate

    Cas No: 51101-09-8

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51101-09-8 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 5-hydroxy-3-mercapto-1,2,4-triazine-6-carboxylate is used as a synthetic intermediate for the development of pharmaceuticals, leveraging its unique chemical structure to contribute to the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, ethyl 5-hydroxy-3-mercapto-1,2,4-triazine-6-carboxylate serves as a key intermediate in the synthesis of various agrochemicals, potentially enhancing crop protection and yield.
Used in Organic Compounds Synthesis:
ethyl 5-hydroxy-3-Mercapto-1,2,4-triazine-6-carboxylate is utilized as a building block in the synthesis of a range of organic compounds, thanks to its reactive functional groups and structural diversity.
Used in Medicinal Chemistry Research:
Ethyl 5-hydroxy-3-mercapto-1,2,4-triazine-6-carboxylate is employed in medicinal chemistry research to explore its interactions with biological systems, with the aim of discovering new pharmaceutical properties and applications.
Used in Materials Science:
Its potential applications in materials science are being investigated, where it may contribute to the development of new materials with unique properties, such as those with enhanced reactivity or stability.

Check Digit Verification of cas no

The CAS Registry Mumber 51101-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51101-09:
(7*5)+(6*1)+(5*1)+(4*0)+(3*1)+(2*0)+(1*9)=58
58 % 10 = 8
So 51101-09-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O3S/c1-2-12-5(11)3-4(10)7-6(13)9-8-3/h2H2,1H3,(H2,7,9,10,13)

51101-09-8SDS

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 ethyl 5-oxo-3-sulfanylidene-2H-1,2,4-triazine-6-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 5-oxo-3-thioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylate

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:51101-09-8 SDS

51101-09-8Relevant articles and documents

Pyridotriazines and pyridopyridazines

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Page 18, (2010/01/31)

This invention relates to bicyclic heterocycles that inhibit cyclin-dependent kinase or tyrosine kinase enzymes, or both, and as such are useful to treat cell proliferative disorders such as angiogenesis, atherosclerosis, restenosis, and cancer as well as immunological disorders such as asthma, rheumatoid arthritis, autoimmune diabetes, and graft rejection associated with transplant surgery in mammals.

Pyridotriazines and pyridopyridazines

-

, (2008/06/13)

This invention relates to bicyclic heterocycles that inhibit cyclin-dependent kinase or tyrosine kinase enzymes, or both, and as such are useful to treat cell proliferative disorders such as angiogenesis, atherosclerosis, restenosis, and cancer as well as immunological disorders such as asthma, rheumatoid arthritis, autoimmune diabetes, and graft rejection associated with transplant surgery in mammals.

Synthesis of 2,4-Dimethylthiobenzonaphthyridin-5(6H)-one: A Potentially Useful Intermediate for the Synthesis of Pyridoacridine Alkaloids

Simth, Kenneth L.,Ray, Partha S.

, p. 11 - 14 (2007/10/03)

Synthesis of the titled benzonaphthyridinone (1) is described using intramolecular inverse electron demand Diels-Alder chemistry of 1,2,4-triazines (10) and (11).

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