127045-27-6

Basic information

• Product Name: 1H-1,2,3-Triazole-4-carboxylicacid,1-amino-5-(methylthio)-,ethylester(9CI)
• Synonyms: 1H-1,2,3-Triazole-4-carboxylicacid,1-amino-5-(methylthio)-,ethylester(9CI)
• CAS NO: 127045-27-6
• Molecular Formula: C₆H₁₀N₄O₂S
• Molecular Weight: 0
• Product Categories: AMINOACID
• Mol File: 127045-27-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-1,2,3-Triazole-4-carboxylicacid,1-amino-5-(methylthio)-,ethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole-4-carboxylicacid,1-amino-5-(methylthio)-,ethylester(9CI)(127045-27-6)
• EPA Substance Registry System: 1H-1,2,3-Triazole-4-carboxylicacid,1-amino-5-(methylthio)-,ethylester(9CI)(127045-27-6)

Safety Data

• Hazardous Substances Data: 127045-27-6(Hazardous Substances Data)

Usage

Chemical structure

1H-1,2,3-Triazole-4-carboxylic acid, 1-amino-5-(methylthio)-, ethyl ester

Triazole ring

A five-membered ring with three nitrogen atoms and two carbon atoms

Carboxylic acid

A functional group containing a carbonyl group (C=O) and a hydroxyl group (-OH) attached to the same carbon atom

Amino group

A functional group containing a nitrogen atom bonded to two hydrogen atoms (-NH2)

Methylthio group

A functional group containing a sulfur atom bonded to a methyl group (-SCH3)

Ethyl ester

A functional group containing an ester linkage (-COO-) with an ethyl group (-CH2CH3) attached to the oxygen atom

Organic synthesis

Used as a building block for the preparation of various heterocyclic compounds

Pharmaceutical research

Used in the development of potential drug candidates

Antimicrobial

Exhibits properties that can inhibit the growth of microorganisms

Anti-cancer

Shows potential in inhibiting the growth and proliferation of cancer cells

Anti-inflammatory

Demonstrates the ability to reduce inflammation in biological systems

Easier handling

The ethyl ester form allows for easier manipulation in laboratory settings

Versatility

Can be used in a wide range of chemical and pharmaceutical research applications

Upstream product

• 126337-28-8 1-amino-4-ethoxycarbonyl-1,2,3-triazole-5-thiol (hydrazinium salt) 
• 74-88-4 methyl iodide 

Downstream Products

• 127045-29-8 1-benzylideneamino-4-ethoxycarbonyl-5-methylmercapto-1,2,3-triazole 

Relevant articles and documents

Dimroth Rearrangement of 5-Hydrazino-1,2,3-thiadiazoles

The reversible isomerization of 5-hydrazino-1,2,3-thiadiazoles and 1-amino-5-mercapto-1,2,3-triazoles has been established for an ester function at the 4-position (4a 5a).Thus, 4a was isolated by reacting 3a with two equivalents of hydrazine, whereas