99417-89-7

Basic information

• Product Name: 1H-1,2,3-Triazole-4-carboxamide,5-mercapto-
• Synonyms: 1H-1,2,3-Triazole-4-carboxamide,5-mercapto-;1H-1,2,3-Triazole-4-carboxamide,5-mercapto-(9CI)
• CAS NO: 99417-89-7
• Molecular Formula: C3H4N4OS
• Molecular Weight: 144.15506
• Product Categories: AMIDE;THIOL
• Mol File: 99417-89-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-1,2,3-Triazole-4-carboxamide,5-mercapto-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole-4-carboxamide,5-mercapto-(99417-89-7)
• EPA Substance Registry System: 1H-1,2,3-Triazole-4-carboxamide,5-mercapto-(99417-89-7)

Safety Data

• Hazardous Substances Data: 99417-89-7(Hazardous Substances Data)

Usage

Structure

A five-membered aromatic ring with three nitrogen atoms (1,2,3-triazole), a carboxamide group, and a mercapto (thiol) group.

Derivative

It is a derivative of 1,2,3-triazole.

Potential applications

Medicinal chemistry, drug development, pharmaceuticals, materials science, and coordination chemistry.

Mercapto group

High affinity for binding to metal ions and can participate in redox reactions.

Aromatic ring

The five-membered ring contributes to the compound's stability and potential reactivity.

Nitrogen atoms

The presence of three nitrogen atoms in the ring enhances the compound's reactivity and potential for forming complexes.

Carboxamide group

Adds functionality to the molecule, allowing for further chemical modifications and potential interactions with biological targets.

Versatility

The combination of the triazole ring, carboxamide, and mercapto groups makes the compound suitable for various applications in different fields.

Redox reactions

The mercapto group's ability to participate in redox reactions adds to the compound's potential uses in chemical and biological processes.

Upstream product

• 153596-16-8 bis(4-ethoxycarbonyl-1,2,3-triazol-5-yl) disulfide 
• 153596-17-9 bis(4-carbamoyl-1,2,3-triazol-5-yl) disulfide 
• 85059-20-7 4-carbamoyl-5-amino-1,2,3-thiadiazole 

Downstream Products

• 107487-63-8 5-Methylthio-1H-1,2,3-triazole-4-carboxamide 
• 100097-66-3 5-amino-1,2,3-thiadiazole-4-carbothioamide 

Relevant articles and documents

ANOMALOUS REARRANGEMENT OF 1,2,3-THIADIAZOLES TO 1,2,3-TRIAZOLES

The rearrangement of 5-amino-1,2,3-thiadiazoles under the influence of halogen-containing oxidizing to bis(triazolyl) disulfides was observed.Ammonia reduces the disulfides obtained to 5-mercapto-1,2,3-triazoles.

RECYCLIZATION OF 5-AMINO-1,2,3-THIADIAZOLE-4-CARBOTHIOAMIDES

-