612483-08-6

Basic information

• Product Name: 2-(5-benzyloxy-2-bromo-4-methoxyphenyl)-1,3-dioxane
• Synonyms: 2-(5-benzyloxy-2-bromo-4-methoxyphenyl)-1,3-dioxane
• CAS NO: 612483-08-6
• Molecular Weight: 379.25
• Mol File: 612483-08-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(5-benzyloxy-2-bromo-4-methoxyphenyl)-1,3-dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-benzyloxy-2-bromo-4-methoxyphenyl)-1,3-dioxane(612483-08-6)
• EPA Substance Registry System: 2-(5-benzyloxy-2-bromo-4-methoxyphenyl)-1,3-dioxane(612483-08-6)

Safety Data

• Hazardous Substances Data: 612483-08-6(Hazardous Substances Data)

Upstream product

• 6451-86-1 5-benzyloxy-2-bromo-4-methoxybenzaldehyde 
• 504-63-2 trimethyleneglycol 

Downstream Products

• 612483-06-4 [(E)-2-(4-Benzyloxy-2-[1,3]dioxan-2-yl-5-methoxy-phenyl)-2-(4-benzyloxy-phenyl)-vinyl]-methyl-((R)-1-phenyl-ethyl)-amine 
• 612483-07-5 4,4'-dibenzyloxy-62(1,3-dioxanyl)-3-methoxybenzophenone 
• 612483-09-7 2-[5-benzyloxy-2-(4-benzyloxyphenylhydroxymethyl)-4-methoxy]-1,3-dioxane 

Relevant articles and documents

A new synthesis of (+)- and (-)-cherylline.

A new and concise synthesis of enantiopure antipodes of alkaloid cherylline has been devised. The synthetic strategy relies upon the reduction of a diversely and polyprotected diarylenamine bearing a chiral auxiliary. Separation of diastereopure intermediates, concomitant deprotections and intramolecular reductive amination complete the synthesis of the natural (S)-enantiomer and of the unnatural (R)-configured antipode.