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Benzenecarbodithioic acid, 3-methyl, methyl ester, also known as 3-Methylbenzenecarbodithioic acid methyl ester or Methyl 3-methylbenzenecarbodithioate, is an organic compound with the chemical formula C9H10S2. It is a colorless to pale yellow liquid with a pungent odor. Benzenecarbodithioic acid, 3-methyl-, methyl ester is primarily used as a fungicide, specifically as a seed treatment agent, to protect crops from various fungal diseases. It is effective against soil-borne diseases and is known for its systemic action, meaning it can be absorbed by the plant and transported to the affected areas. The compound is also used in the synthesis of other chemicals and as an intermediate in the production of rubber chemicals. It is important to handle this chemical with care due to its potential toxicity and environmental impact.

5969-49-3

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5969-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5969-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5969-49:
(6*5)+(5*9)+(4*6)+(3*9)+(2*4)+(1*9)=143
143 % 10 = 3
So 5969-49-3 is a valid CAS Registry Number.

5969-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-methylbenzenecarbodithioate

1.2 Other means of identification

Product number -
Other names Methyl dithio-3-methylbenzoate

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:5969-49-3 SDS

5969-49-3Relevant academic research and scientific papers

Discovery of Pyrazolocarboxamides as Potent and Selective Receptor Interacting Protein 2 (RIP2) Kinase Inhibitors

Haffner, Curt D.,Charnley, Adam K.,Aquino, Christopher J.,Casillas, Linda,Convery, Máire A.,Cox, Julie A.,Elban, Mark A.,Goodwin, Nicole C.,Gough, Peter J.,Haile, Pamela A.,Hughes, Terry V.,Knapp-Reed, Beth,Kreatsoulas, Constantine,Lakdawala, Ami S.,Li, Huijie,Lian, Yiqian,Lipshutz, David,Mehlmann, John F.,Ouellette, Michael,Romano, Joseph,Shewchuk, Lisa,Shu, Arthur,Votta, Bartholomew J.,Zhou, Huiqiang,Bertin, John,Marquis, Robert W.

, p. 1518 - 1523 (2019)

Herein we report the discovery of pyrazolocarboxamides as novel, potent, and kinase selective inhibitors of receptor interacting protein 2 kinase (RIP2). Fragment based screening and design principles led to the identification of the inhibitor series, and X-ray crystallography was used to inform key structural changes. Through key substitutions about the N1 and C5 N positions on the pyrazole ring significant kinase selectivity and potency were achieved. Bridged bicyclic pyrazolocarboxamide 11 represents a selective and potent inhibitor of RIP2 and will allow for a more detailed investigation of RIP2 inhibition as a therapeutic target for autoinflammatory disorders.

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