114722-63-3

Basic information

• Product Name: ([1,2,4]TRIAZOLO[3,4-B][1,3]BENZOTHIAZOL-3-YLTHIO)ACETIC ACID
• Synonyms: AKOS BC-3151;([1,2,4]TRIAZOLO[3,4-B][1,3]BENZOTHIAZOL-3-YLTHIO)ACETIC ACID;IFLAB-BB F0307-0305;(Benzo[4,5]thiazolo[2,3-c][1,2,4]triazol-3-ylsulfanyl)-acetic acid;2-(benzo[4,5]thiazolo[2,3-c][1,2,4]triazol-3-ylthio)acetic acid
• CAS NO: 114722-63-3
• Molecular Formula: C10H7N3O2S2
• Molecular Weight: 265.31
• Mol File: 114722-63-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ([1,2,4]TRIAZOLO[3,4-B][1,3]BENZOTHIAZOL-3-YLTHIO)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: ([1,2,4]TRIAZOLO[3,4-B][1,3]BENZOTHIAZOL-3-YLTHIO)ACETIC ACID(114722-63-3)
• EPA Substance Registry System: ([1,2,4]TRIAZOLO[3,4-B][1,3]BENZOTHIAZOL-3-YLTHIO)ACETIC ACID(114722-63-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 114722-63-3(Hazardous Substances Data)

Usage

Uses

(Benzo[4,5]thiazolo[2,3-c][1,2,4]triazol-3-ylsulfanyl)-acetic acid is a reactant used in the synthesis of polyazaindenes and related compounds.

Upstream product

• 6957-85-3 2H-benzo[4,5]thiazolo[2,3-c][1,2,4]triazole-3-thione 
• 3926-62-3 sodium monochloroacetic acid 
• 6957-85-3 [1,2,4]-triazolo[3,4-b][1,3]benzothiazole-3-thiol 
• 79-11-8 chloroacetic acid 
• 40527-73-9 ethyl S-triazolo[3,4-b]benzothiazol-3-ylthioacetate 
• 149-30-4 2-Mercaptobenzothiazole 
• 615-21-4 1,3-benzothiazol-2-ylhydrazine 

Downstream Products

• 1423012-41-2 s-triazolo[3,4-b]benzothiazole-3-thioacetyl (L)-methionine methyl ester 
• 1423012-42-3 C₂₃H₂₉N₅O₂S₂ 

Relevant articles and documents

Synthesis and antifungal activity of some s-mercaptotriazolobenzothiazolyl amino acid derivatives

A series of s-triazolobenzothiazolylthioacetyl/propionyl amino acid derivatives were synthesized with the aim of evaluating their antifungal activity. Their chemical structures were confirmed by 1H, 13C NMR, IR, mass spectrometry and elemental analyses. The synthesized derivatives were screened for their antifungal activity against Aspergillus flavus and Candida albicans. Five compounds (3, 5, 7c, 8 and 17) were found to possess high activity comparable to fluconazole at 100 μg/mL against C. albicans.