78283-38-2

Upstream product

• 67127-91-7 2,5-bis(benzyloxy)benzoic acid 
• 100-44-7 benzyl chloride 
• 490-79-9 2,5-dihydroxybenzoic acid. 
• 106296-25-7 methyl 2,5-bis(phenylmethoxy)benzoate 
• 78283-37-1 benzyl 2,5-bis(benzyloxy)benzoate 

Downstream Products

• 78283-39-3 2,5-bisbenzyloxybenzyl chloride 
• 106295-98-1 2,5-dibenzyloxybenzyl bromide 
• 79755-47-8 2,5-bisbenzyloxyphenylacetic acid 
• 79755-48-9 1-(2,5-bisbenzyloxyphenyl)propan-2-one 
• 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 
• 78311-08-7 5,8-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline 
• 79357-92-9 5,8-dihydroxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 78283-42-8 N-(2,5-dibenzyloxyphenethyl)-2-(3,4,5-trimethoxyphenyl)acetamide 
• 78283-40-6 2,5-bisbenzyloxybenzyl cyanide 
• 106295-99-2 2-(2,5-Bis-benzyloxy-benzyl)-malonic acid diethyl ester 
• 106296-00-8 2-(2,5-Bis-benzyloxy-benzyl)-malonic acid 

Relevant academic research and scientific papers

Charge Separation in Carotenoporphyrin-Quinone Triads: Synthetic, Conformational, and Fluorescence Lifetime Studies

Carotenoid-porphyrin-quinone triad molecules undergo a photodriven two-step electron-transfer reaction which results in the generation of a high-energy charge-separated state with a lifetime on the microsecond time scale at ambient temperatures in fluid s

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.