137761-44-5

Upstream product

• 75-15-0 carbon disulfide 
• 696-60-6 4-aminomethylphenol 
• 74-88-4 methyl iodide 
• 137761-45-6 4-aminomethyl-phenol; hydriodide 
• 767-00-0 4-cyanophenol 
• 22171-15-9 4-(benzyloxy)benzylamine 
• 52805-36-4 4-benzyloxybenzonitrile 

Downstream Products

• 137761-62-7 N-(4-hydroxybenzyl)-thiosemicarbazide 

Relevant academic research and scientific papers

Sinalexin, a phytoalexin from white mustard elicited by destruxin B and Alternaria brassicae

Determination of the structure of sinalexin, a phytoalexin produced by white mustard (Sinapis alba) under biotic or abiotic elicitation, is described. Additionally, the isolation and synthesis of 4- hydroxybenzylisothiocyanate, the major antifungal component isolated from extracts of white mustard, and optimized conditions for the isolation of the phytotoxin destruxin B are described.

Preparation, biotransformation, and antifungal activity of methyl benzyldithiocarbamates

The biotransformation of three methyl benzyldithiocarbamates by the blackleg fungus (Leptosphaeria maculans (Desm.) Ces. et de Not., asexual stage Phoma lingam (Tode ex Fr.) Desm) was investigated. The main biotransformation products were isolated and their chemical structures were determined by spectroscopic methods. Similarly to our previous studies with the phytoalexin brassinin, these results suggest that virulent blackleg isolates are significantly more effective in metabolizing benzyldithiocarbamates than the related avirulent isolates. The biotransformation of three methyl benzyldithiocarbamates by the blackleg fungus (Leptosphaeria maculans (Desm.) Ces. et de Not., asexual stage Phoma lingam (Tode ex Fr.) Desm) was investigated. The main biotransformation products were isolated and their chemical structures were determined by spectroscopic methods. Similarly to our previous studies with the phytoalexin brassinin, these results suggest that virulent blackleg isolates are significantly more effective in metabolizing benzyldithiocarbamates than the related avirulent isolates.

TRIAZOLE ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT

Substituted triazoles attached through a methylene bridge to novel substituted phenyl derivatives of the Formula I, are useful as angiotensin II antagonists. STR1