304662-70-2

Basic information

• Product Name: 2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE
• Synonyms: AURORA 22568;2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE;AKOS BBS-00008005
• CAS NO: 304662-70-2
• Molecular Formula: C4H6N4OS2
• Molecular Weight: 190.25
• Mol File: 304662-70-2.mol

Chemical Properties

• Boiling Point: 494.0±47.0 °C(Predicted)
• Appearance: /
• Density: 1.62±0.1 g/cm3(Predicted)
• PKA: 14.97±0.40(Predicted)
• CAS DataBase Reference: 2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE(304662-70-2)
• EPA Substance Registry System: 2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE(304662-70-2)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 304662-70-2(Hazardous Substances Data)

Usage

Derivatives

Thiadiazole and acetamide The compound is derived from two main parent compounds, namely thiadiazole and acetamide.

Thioamide functional group

Present The compound contains a thioamide group (S-C=N) which is a sulfur analog of an amide group.

Five-membered ring structure

Nitrogen and sulfur atoms The compound features a five-membered heterocyclic ring containing both nitrogen and sulfur atoms, which contributes to its unique chemical properties.

Amino group attachment

Thiadiazole ring An amino group (-NH2) is attached to the thiadiazole ring, contributing to the compound's basic properties.

Basic properties

Amino group The presence of the amino group makes the compound basic, meaning it can accept a proton (H+) in a chemical reaction.

Potential applications

Pharmaceuticals and organic synthesis Due to its unique structural features, 2-(5-AMINO-[1,3,4]THIADIAZOL-2-YLSULFANYL)-ACETAMIDE may have possible uses in the pharmaceutical industry and organic synthesis for creating new compounds.

Structural uniqueness

Combination of functional groups The compound's unique structure comes from the combination of thiadiazole, acetamide, thioamide, and amino functional groups, which may contribute to its potential applications in various fields.

Upstream product

• 143599-42-2 N-(2-Amino-1,3,4-thiadiazol-5-ylthioacetyl)methylcarbamate Hydrochloride 

Relevant articles and documents

Synthesis and anthelmintic activity of carbamates derived from imidazo[2,1-b][1,3,4]thiadiazole and imidazo[2,1-b]thiazole

The anthelmintic activity of 25 compounds, most of them carbamates, was determined. The in vitro results are interesting and show that an aromatic azapentalene can replace the benzimidazole ring without loss of its biological properties. The in vivo resul