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18212-21-0

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18212-21-0 Usage

Description

4-Methyl-1,2,3-thiadiazole-5-carboxylic acid is an organic compound characterized by a white to light yellow crystalline powder. It features a unique chemical structure that includes a thiadiazole ring with a methyl group and a carboxylic acid functional group, which contributes to its diverse range of applications.

Uses

Used in Agrochemical Industry:
4-Methyl-1,2,3-thiadiazole-5-carboxylic acid is used as an active ingredient in agrochemicals for its antiviral, fungicidal, and insecticidal properties. Its ability to combat various pathogens and pests helps protect crops and improve agricultural yields.
In the Agrochemical Industry, 4-Methyl-1,2,3-thiadiazole-5-carboxylic acid is used as an antiviral agent to protect plants from viral infections, ensuring healthier growth and higher crop quality.
4-Methyl-1,2,3-thiadiazole-5-carboxylic acid is also used as a fungicide, effectively controlling fungal infections that can damage crops and reduce yields.
Additionally, 4-Methyl-1,2,3-thiadiazole-5-carboxylic acid is used as an insecticide, targeting pests that threaten the productivity and quality of crops.

Check Digit Verification of cas no

The CAS Registry Mumber 18212-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,1 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18212-21:
(7*1)+(6*8)+(5*2)+(4*1)+(3*2)+(2*2)+(1*1)=80
80 % 10 = 0
So 18212-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2O2S/c1-2-3(4(7)8)9-6-5-2/h1H3,(H,7,8)/p-1

18212-21-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (B20449)  4-Methyl-1,2,3-thiadiazole-5-carboxylic acid, 98%   

  • 18212-21-0

  • 5g

  • 1236.0CNY

  • Detail
  • Alfa Aesar

  • (B20449)  4-Methyl-1,2,3-thiadiazole-5-carboxylic acid, 98%   

  • 18212-21-0

  • 25g

  • 5191.0CNY

  • Detail
  • Alfa Aesar

  • (B20449)  4-Methyl-1,2,3-thiadiazole-5-carboxylic acid, 98%   

  • 18212-21-0

  • 100g

  • 17285.0CNY

  • Detail
  • Aldrich

  • (703397)  4-Methyl-1,2,3-thiadiazole-5-carboxylicacid  97%

  • 18212-21-0

  • 703397-1G

  • 325.26CNY

  • Detail
  • Aldrich

  • (703397)  4-Methyl-1,2,3-thiadiazole-5-carboxylicacid  97%

  • 18212-21-0

  • 703397-5G

  • 1,068.21CNY

  • Detail

18212-21-0SDS

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 4-methylthiadiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-5-hydroxycarbonyl-1,2,3-thiadiazole

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:18212-21-0 SDS

18212-21-0Relevant articles and documents

Design, synthesis, and evaluation of substituted 2-acylamide-1,3-benzo[d]zole analogues as agents against MDR- and XDR-MTB

Li, Dongsheng,Liu, Chao,Jiang, Xinhai,Lin, Yuan,Zhang, Jing,Li, Yan,You, Xuefu,Jiang, Wei,Chen, Minghua,Xu, Yanni,Si, Shuyi

, (2020/10/21)

N-(5-Chlorobenzo[d]oxazol-2-yl)-4-methyl-1,2,3-thiadiazole-5-carboxamideox-amide has been identified as a potent inhibitor of Mtb H37Rv, with a minimum inhibitory concentration (MIC) of 0.42 μM. In this study, a series of substituted 2-acylamide-1,3-zole analogues were designed and synthesized, and their anti-Mtb activities were analyzed. In total, 17 compounds were found to be potent anti-Mtb agents, especially against the MDR- and XDR-MTB strains, with MIC values 10 μM. These analogues can inhibit both drug-sensitive and drug-resistant Mtb. Four representative compounds were selected for further profiling, and the results indicate that compound 18 is acceptably safe and has favorable pharmacokinetic (PK) properties. In addition, this compound displays potent activity against Gram-positive bacteria, with MIC values in the range of 1.48–11.86 μM. The data obtained herein suggest that promising anti-Mtb candidates may be developed via structural modification, and that further research is needed to explore other compounds.

Substituted benzo - 1, 3 - [...] compound, its preparation and use

-

Paragraph 0092; 0093; 0094, (2017/04/21)

The invention relates to a substituted benzo-1, 3-miscellaneous azole compound shown in the general formula I, and further relates to a preparation method of the compound and application to the preparation of antituberculosis drugs. The compound provided by the invention has effect not only on mycobacterium tuberculosis sensitive strains, but also on resistant strains which have drug resistance to isoniazid, rifampicin, and other traditional frontline antituberculosis drugs, and is a novel antimycobacterium tuberculosis compound.

guan Huanfa synthetic multi-nitrogen heterocyclic ring sai oxadiazole - 5 - a amidine compounds

-

Paragraph 0049, (2017/07/21)

The invention discloses an N-trisubstituted-1,2,3-thiadiazoles-5-formamidine target compound of which the general formula is TDCA. The N-trisubstituted-1,2,3-thiadiazoles-5-formamidine target compound is obtained from an M compound through a cyclization reaction. The new synthetizing method is high in yield, catalysts are easy to prepare, the catalysts are low in cost, phosphoric waste water is less, and the multi-nitrogen heterocycle thiadiazoles-5-formamidine compound is environment-friendly. (As shown in the Description).

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