79755-47-8

Usage

Physical form

White to off-white crystalline powder

Solubility

Insoluble in water, soluble in organic solvents

Uses

Synthesis of pharmaceutical and agrochemical products, production of fragrances and flavoring agents

Medicinal properties

Anti-inflammatory and analgesic

Chemical applications

Chemical intermediate in the production of various fine chemicals, potential applications in the field of organic chemistry.

Upstream product

• 78283-40-6 2,5-bisbenzyloxybenzyl cyanide 
• 67127-91-7 2,5-bis(benzyloxy)benzoic acid 
• 490-79-9 2,5-dihydroxybenzoic acid. 
• 78283-37-1 benzyl 2,5-bis(benzyloxy)benzoate 
• 78283-39-3 2,5-bisbenzyloxybenzyl chloride 
• 78283-38-2 2,5-bisbenzyloxybenzyl alcohol 
• 100-44-7 benzyl chloride 

Downstream Products

• 79755-55-8 1-(3,5-bisbenzyloxyphenyl)-2-chloropropane 
• 79755-56-9 1-(3,5-dihydroxyphenyl)-2-chloropropane 
• 79755-57-0 1-(3,5-dihydroxyphenyl)prop-1-ene 
• 34701-77-4 1-(2,5-dihydroxyphenyl)propan-2-one 
• 79755-48-9 1-(2,5-bisbenzyloxyphenyl)propan-2-one 

Relevant academic research and scientific papers

Amide compounds, their production and use

A compound is provided which has the formula STR1 wherein m is an integer of 1 to 3; n is an integer of 1 or 2; p is an integer of 1 or 2; q is an integer of 1 to 6; x is an integer of 2 to 6; Ph is phenylene or a pharmceutically acceptable salt thereof. Also provided is a method for glutamate receptor inhibition which comprises administering to a mammal in need thereof an effective amount of said compound or a pharmaceutically acceptable salt thereof. Compositions for glutamate receptor inhibition are provided which contain an effective amount of said compound to provide a glutamate receptor inhibition effect, together with at least one pharmaceutically acceptable carrier, dilient or excipient therefor.

Biosynthesis of Fungal Metabolites. Terrein, a Metabolite of Aspergillus terreus Thom

Terrein, a metabolite of Aspergillus terreus Thom, is biosynthesised from 3,4-dihydro-6,8-dihydroxy-3-methylisocoumarin by contraction of an aryl ring.The direction of the ring contraction has been investigated using acetate as precursor.