141542-10-1

Basic information

• Product Name: 1,2,5-Thiadiazol-3-amine, 4,5-dihydro-4-phenyl-, 1,1-dioxide
• CAS NO: 141542-10-1
• Molecular Formula: C8H9N3O2S
• Molecular Weight: 211.244
• Mol File: 141542-10-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,2,5-Thiadiazol-3-amine, 4,5-dihydro-4-phenyl-, 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,5-Thiadiazol-3-amine, 4,5-dihydro-4-phenyl-, 1,1-dioxide(141542-10-1)
• EPA Substance Registry System: 1,2,5-Thiadiazol-3-amine, 4,5-dihydro-4-phenyl-, 1,1-dioxide(141542-10-1)

Safety Data

• Hazardous Substances Data: 141542-10-1(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, nitrogen and sulfur.

Explanation

The compound contains both nitrogen and sulfur atoms in its structure, contributing to its unique properties.

Explanation

Due to its unique chemical properties and reactivity, the compound has potential applications in the development of drugs for various therapeutic purposes.

Explanation

The presence of these functional groups contributes to the compound's unique chemical properties and reactivity.

Explanation

Investigating the compound's potential uses and properties could lead to the discovery of new pharmaceutical agents or other useful applications.

Explanation

The compound exhibits unique chemical properties and reactivity due to the presence of the thiadiazole and amine functional groups.

Heterocyclic compound

Yes

Nitrogen and sulfur atoms

Present

Pharmaceutical industry applications

Potential

Thiadiazole and amine functional groups

Present

Further research and study

Recommended

Chemical properties and reactivity

Unique

Upstream product

• 773837-37-9 sodium cyanide 
• 100-52-7 benzaldehyde 
• 134-81-6 benzil 
• 143-33-9 sodium cyanide 
• 1074-12-0 phenylglyoxal hydrate 
• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 151-50-8 potassium cyanide 

Downstream Products

• 120991-36-8 4-phenyl-3-oxo-1,2,5-thiadiazolidine 1,1-dioxide 
• 120991-40-4 2,5-dimethyl-3-(N-methylimino)-4-phenyl-1,2,5-thiadiazolidine 1,1-dioxide 
• 2835-06-5 phenylglycin 
• 120991-32-4 ethyl α-sulfamidophenylacetate 
• 120991-38-0 3-(N-benzylamino)-4-phenyl-4,5-dihydro-1,2,5-thiadiazole 1,1-dioxide 

Relevant articles and documents

Microwave-assisted synthesis of some substituted sulfamides

Microwave-assisted synthesis of some substituted open-chain and cyclic sulfamides, by amine-exchange reaction, was studied in a modified domestic microwave oven. Reaction times and yields under microwave radiation were compared with classical heating. Synthesis of the sulfamides under microwave irradiation gave better yields with the desired compounds, and in considerably reduced reaction times, than those obtained by classical heating. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional figures.]