13980-80-8

Upstream product

• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 86-93-1 1-phenyl-1H-tetrazole-5-thiol 
• 13980-78-4 ethyl α-[5-(1-phenyltetrazolyl)thio]acetate 
• 3206-49-3 methyl (1-phenyltetrazol-5-ylthio)acetate 

Downstream Products

• 1231978-03-2 5-(1-phenyl-1H-tetrazol-5-ylsulfanylmethyl)-N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-1,3,4-oxadiazol-2-amine 
• 1231978-04-3 5-(1-phenyl-1H-tetrazol-5-ylsulfanylmethyl)-N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-1,3,4-thiadiazol-2-amine 
• 1231978-21-4 5-(1-phenyl-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-oxadiazol-2-amine 
• 1231978-22-5 5-(1-phenyl-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine 
• 1231978-42-9 N'-[N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)thiocarbamoyl]-2-(1-phenyl-1H-tetrazol-5-ylsulfanyl)acetohydrazide 
• 133506-48-6 C₁₆H₁₅N₇OS₂ 
• 1574548-89-2 N'-[(4-cyanophenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-88-1 N'-[(4-bromophenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-87-0 N'-[(4-chlorophenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-86-9 N'-[(4-fluorophenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-85-8 N'-[(4-methoxyphenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-84-7 N'-[(4-methylphenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-83-6 N'-[(4-nitrophenyl-3-phenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 
• 1574548-82-5 N'-[(3,4-diphenylthiazol-2(3H)-ylidene)]-2-[(1-phenyl-1H-tetrazol-5-yl)thio]acetohydrazide 

Relevant academic research and scientific papers

Synthesis and evaluation of tetrazole-based hydrazone derivatives bearing a pyridine moiety as antimicrobial agents

2-[(1-Methyl/Phenyl-1 H-tetrazol-5-yl)thio]-N '-[(aryl)methylidene/ethylidene]acetohydrazides were synthesized and investigated in vitro against pathogenic bacteria and Candida species for their antimicrobial activity using CLSI broth microdilution method

Synthesis and biological evaluation of thiazoline derivatives as new antimicrobial and anticancer agents

N′-(3,4-Diarylthiazol-2(3H)-ylidene)-2-(arylthio)acetohydrazides were synthesized and evaluated for their antimicrobial activity and cytotoxicity against NIH/3T3 cells. Compound 22 bearing 1-phenyl-1H-tetrazole and p-chlorophenyl moieties was found to be

Synthesis and bioactivity of 5-(1-aryl-1H-tetrazol-5-ylsulfanylmethyl)-N- xylopyranosyl-1,3,4-oxa(thia)diazol-2-amines

A series of new N′-[N-(2,3,4-tri-O-acetyl-β-d-xylopyranosyl) thiocarbamoyl]-2-[(1-aryl-1H-tetrazol-5-yl)sulfanyl]acetohydrazides 5a-5e were synthesized rapidly in high yields from 2-(1-aryl-1H-tetrazol-5-ylsulfanyl) acetohydrazides 3a-3e and 2,3,4-tri-O-a

Efficient synthesis of 1-substituted-4-phenyl-1,4-dihydro-5H-tetrazole-5- thione and (1-Phenyl-1H-tetrazol-5-yl)thioacetyl derivatives

A new and convenient synthesis of a variety of N- and S-substituted tetrazoles has been developed via azide and Mannich reaction methods. Compounds were characterized by elemental analysis, MALDI MS, and 1H NMR data.

ANTIMYCOBACTERIAL DERIVATIVES OF TETRAZOLE

A synthesis of (1-phenyltetrazol-5-ylthio)acetic acid derivatives has been developed.Functional variations concern the carboxylic group and/or the 4 position of phenyl group.Most of the compounds prepared have been tested with regard to their antimycobact