98110-81-7

Upstream product

• 121-33-5 vanillin 
• 13278-67-6 4-(4-methylphenyl)-3-thiosemicarbazide 
• 622-59-3 1-isothiocyanato-4-methylbenzene 

Downstream Products

• 98654-77-4 4-hydroxy-3-methoxy-benzaldehyde (4-oxo-3-p-tolyl-thiazolidin-2-ylidene)-hydrazone 
• 98999-68-9 4-hydroxy-3-methoxy-benzaldehyde (5-methyl-4-oxo-3-p-tolyl-thiazolidin-2-ylidene)-hydrazone 
• 92968-64-4 2-(3-methoxy-4-hydroxyphenyl)-5-(4-methylphenylamino)-1,3,4-thiadiazole 
• 1380074-96-3 N¹-4-methylbenzylidene-N²-[3-(4-hydroxy-3-methoxyphenyl)-4-(2,5-dihydroxyphenyl)-1,3-thiazol-2-ylidene]hydrazine 
• 1380075-14-8 N¹-4-methylbenzylidene-N²-[3-(4-hydroxy-3-methoxyphenyl)-4-(1,4-benzoquinon-2-yl)-1,3-thiazol-2-ylidene]hydrazine 
• 101656-62-6 4-hydroxy-3-methoxy-benzaldehyde (4-oxo-5-phenyl-3-p-tolyl-thiazolidin-2-ylidene)-hydrazone 

Relevant academic research and scientific papers

Synthesis and biological evaluation of novel benzoquinones as potential antimicrobial agents

New series of 2,5-dihydroxyphenyl-1,3-thiazoles 4a-l was synthesized by reacting 2,5-dihydroxyphenacyl bromide with various 4-aryl thiosemicarbazones 3a-l that on oxidation with ferric chloride yielded the corresponding N 1-substituted benzylid

One-pot synthesis and anticancer studies of 2-arylamino-5-aryl-1,3,4- thiadiazoles

A series of 2-arylamino-5-aryl-1,3,4-thiadiazoles 1a-j were synthesized and screened for their anticancer activity against various human cancer cell lines. The novel one-pot synthesis of 1,3,4-thiadiazoles was achieved by refluxing aryl aldehydes, hydrazi