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17467-60-6

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17467-60-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon atoms, 11 hydrogen atoms, 5 nitrogen atoms, and 1 sulfur atom.

Explanation

The compound belongs to the thiadiazole family, which is a group of chemical compounds characterized by a five-membered ring containing four carbon atoms, one nitrogen atom, and one sulfur atom.

Explanation

The thiadiazole ring is a five-membered structure with the specified atoms. The compound has an amine group (-NH2) and two phenyl groups (C6H5) attached to one of the nitrogen atoms in the ring.

Explanation

The compound is used in the synthesis of other organic compounds and has potential applications in the development of pharmaceuticals and agrochemicals due to its unique structure and properties.

Explanation

Thiadiazole compounds, including this specific compound, have been studied for their diverse biological activities. These activities make them of interest for further research and development in the fields of medicine and pharmaceuticals.

Explanation

Due to its unique structure and potential biological activities, the compound may be useful in the development of new pharmaceuticals and agrochemicals, warranting further research and development in these areas.

Family

Thiadiazole

Structure

Five-membered ring with an amine group and two phenyl groups attached to the nitrogen atom

Applications

Organic synthesis and medicinal chemistry

Biological activities

Antimicrobial, antiviral, and anticancer properties

Potential for further research and development

Pharmaceutical and agrochemical development

Check Digit Verification of cas no

The CAS Registry Mumber 17467-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,6 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17467-60:
(7*1)+(6*7)+(5*4)+(4*6)+(3*7)+(2*6)+(1*0)=126
126 % 10 = 6
So 17467-60-6 is a valid CAS Registry Number.

17467-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,3-Diphenyl-1,2,4-thiadiazol-5-amine

1.2 Other means of identification

Product number -
Other names HMS2896L09

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:17467-60-6 SDS

17467-60-6Relevant articles and documents

H2O2-Mediated Synthesis of 1,2,4-Thiadiazole Derivatives in Ethanol at Room Temperature

Cao, Xian-Ting,Zheng, Zuo-Ling,Liu, Jie,Hu, Yu-He,Yu, Hao-Yun,Cai, Shasha,Wang, Guannan

, p. 689 - 694 (2022/01/11)

Herein, we report the H2O2-mediated synthesis of 1,2,4-thiadiazole derivatives under metal-free conditions at room temperature with ethanol as the sole solvent. Various substrates could undergo the reaction smoothly, providing the ex

Transition-metal-free visible Light-promoted photoredox oxidative dehydrogenative cyclization:expeditious approach to 1,2,4-thiadiazoles

Chen, Junmin,Sheng, Shouri,Xiong, Zhiqiang,Zhong, Qihao

, (2021/09/06)

A novel visible-light-catalyzed oxidative N-S bond formation for the synthesis of 3,5-disubstituted 1,2,4-thiadiazoles has been developed. This protocol features a metal-free approach, green oxidant, room temperature process, broad substrate scope, good functional group tolerance, excellent yields and a one-pot reaction without the isolation of the intermediates.

Electrochemical Oxidative Intramolecular N-S Bond Formation: Synthesis of 3-Substituted 5-Amino-1,2,4-Thiadiazoles

Yang, Zan,Zhang, Jiaqi,Hu, Liping,Li, Lijun,Liu, Kun,Yang, Tao,Zhou, Congshan

, p. 3358 - 3363 (2020/03/23)

A facile and efficient protocol for the synthesis of 3-substituted 5-amino-1,2,4-thiadiazoles has been developed through the electro-oxidative intramolecular dehydrogenative N-S bond formation of imidoyl thioureas. Various 1,2,4-thiadiazole derivatives we

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