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ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE is a chemical compound that belongs to the class of organic compounds known as triazines. Specifically, it is a derivative of 1,2,4-triazine, characterized by the presence of a methylthio group at the third position, a hydroxy group at the fifth position, and a carboxylate group at the sixth position. This unique structure, which contains features such as ether, a carboxylic acid ester, and a sulfide, contributes to a variety of chemical and physical properties. The safety, toxicity, and environmental impact of ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE, like many chemicals, largely depend on its usage and handling practices.

31143-85-8

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31143-85-8 Usage

Uses

Used in Chemical Synthesis:
ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE is used as a reactant or intermediate in various chemical reactions due to its unique structure and properties. Its presence of ether, carboxylic acid ester, and sulfide groups allows for versatile applications in the synthesis of other compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE is used as a building block for the development of new drugs. Its chemical structure can be modified to create potential therapeutic agents, taking advantage of its reactivity and functional groups.
Used in Agrochemical Industry:
ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties make it a valuable component in the development of effective crop protection products.
Used in Material Science:
In material science, ETHYL 5-HYDROXY-3-(METHYLTHIO)-1,2,4-TRIAZINE-6-CARBOXYLATE is used as a component in the development of new materials with specific properties. Its versatility in chemical reactions allows for the creation of materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31143-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,4 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31143-85:
(7*3)+(6*1)+(5*1)+(4*4)+(3*3)+(2*8)+(1*5)=78
78 % 10 = 8
So 31143-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N3O3S/c1-3-13-6(12)4-5(11)8-7(14-2)10-9-4/h3H2,1-2H3,(H,8,10,11)

31143-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methylsulfanyl-5-oxo-2H-1,2,4-triazine-6-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3-(methylsulfanyl)-5-oxo-2,5-dihydro-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:31143-85-8 SDS

31143-85-8Relevant academic research and scientific papers

PYRIMIDINE DERIVATIVES AND THEIR USE USE FOR THE TREATMENT OF CANCER

-

Page/Page column 71-72, (2019/07/13)

Compounds of general formula (I): (Formula (I)) wherein R1, R2, X1 and X2 are as defined herein are useful for the treatment of cancer, particularly solid tumours.

Pyridotriazines and pyridopyridazines

-

, (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 Fused 1,2,4-Triazines: 6- and 7-Azapteridine and 6-Azapurine Ring Systems

Huang, Jim J.

, p. 2293 - 2298 (2007/10/02)

The reaction of diethyl oxomalonate with S-methylisothiosemicarbazide under basic condition was found to give 3-(methylthio)-5-oxo-6-carbethoxy-4,5-dihydro-1,2,4-triazine (1) and 3-(methylthio)-5-carbethoxy-6-oxo-1,6-dihydro-1,2,4-triazine (2).While via 1

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