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6-Methylpyridine-2-thioamide is a heterocyclic aromatic compound with the molecular formula C7H8N2S. It features a sulfur atom at the 2-position and a methyl group at the 6-position within its ring structure.

5933-30-2

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5933-30-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Methylpyridine-2-thioamide is used as a building block for the synthesis of various pharmaceuticals due to its potential biological activities and incorporation in the structure of certain drugs.
Used in Pesticide Industry:
6-methylpyridine-2-thioamide is utilized as a component in the development of pesticides, contributing to the creation of effective and targeted agrochemicals.
Used in Catalyst Industry:
6-Methylpyridine-2-thioamide serves as a key component in the formulation of catalysts, playing a crucial role in various chemical reactions and processes.
Used in Organic Synthesis:
As a versatile building block, 6-methylpyridine-2-thioamide is employed in the synthesis of a wide range of organic compounds for diverse applications across different industries.
Used in Medicinal Research:
6-methylpyridine-2-thioamide holds promise in medicinal research due to its potential biological activities, which are being explored for the development of new therapeutic agents.
Used in Agricultural Applications:
6-Methylpyridine-2-thioamide's potential biological activities also extend to agricultural uses, where it may contribute to the development of treatments and solutions for various crop and livestock issues.

Check Digit Verification of cas no

The CAS Registry Mumber 5933-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5933-30:
(6*5)+(5*9)+(4*3)+(3*3)+(2*3)+(1*0)=102
102 % 10 = 2
So 5933-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2S/c1-5-3-2-4-6(9-5)7(8)10/h2-4H,1H3,(H2,8,10)

5933-30-2SDS

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 6-methylpyridine-2-carbothioamide

1.2 Other means of identification

Product number -
Other names 6-Methylpicolinic acid-thioamide

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:5933-30-2 SDS

5933-30-2Relevant academic research and scientific papers

A efficient protocol for the synthesis of thioamides in [DBUH][OAc] at room temperature

Cao, Xian-Ting,Qiao, Li,Zheng, Hui,Yang, Hui-Yong,Zhang, Peng-Fei

, p. 170 - 175 (2018/01/17)

A novel, simple and eco-friendly method to synthesize thioamides from aryl nitriles and sodium sulfide (Na2S·9H2O) catalyzed by 1,8-diazabicyclo[5,4,0]undec-7-enium acetate ([DBUH][OAc]) ionic liquid (IL) at room temperature was developed in this paper. In this reaction, readily available inorganic salt (Na2S·9H2O) serves as the sulfur source, and various functional groups of aryl nitriles were well tolerated at room temperature. In addition, the products were easily separated from the IL which could be reused at least five times without considerable loss of its activity and applied in the green, concise synthesis of ethionamide.

A simple method for synthesis of thioamides and application in synthesis of 1,2,4-thiadiazoles

Cao, Xian Ting,Yang, Huiyong,Zheng, Hui,Zhang, Pengfei

, p. 509 - 517 (2018/03/27)

A novel, simple protocol is disclosed for the synthesis of 1,2,4-thiadiazoles starting from thioamides with Na2-eosin Y-sensitized titanium dioxide as catalyst through visible light irradiation (7 W blue LED light) and only 0.3 mol% catalysts were used. The raw material thioamides is prepared by aryl nitriles and sodium sulfide (Na2S9H2O) in DMF and in this reaction, readily available, inexpensive inorganic salt (Na2S9H2O) serves as the sulfur source and various functional groups of aryl nitriles were well and thioamides were synthesized successfully in gram-scale.

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