74882-26-1

Basic information

• Product Name: 1,7-bis-(4-methoxyphenyl)-heptan-3-one
• Synonyms: 1,7-bis-(4-methoxyphenyl)-heptan-3-one
• CAS NO: 74882-26-1
• Molecular Weight: 326.436
• Mol File: 74882-26-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,7-bis-(4-methoxyphenyl)-heptan-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,7-bis-(4-methoxyphenyl)-heptan-3-one(74882-26-1)
• EPA Substance Registry System: 1,7-bis-(4-methoxyphenyl)-heptan-3-one(74882-26-1)

Safety Data

• Hazardous Substances Data: 74882-26-1(Hazardous Substances Data)

Upstream product

• 35191-43-6 1-(4-bromo-butyl)-4-methoxy-benzene 
• 105-13-5 4-Methoxybenzyl alcohol 
• 99-96-7 4-hydroxy-benzoic acid 
• 121-98-2 methyl 4-methoxybenzoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 824-94-2 p-methoxybenzyl chloride 
• 100-66-3 methoxybenzene 
• 74893-19-9 4,4,6-trimethyl-2-(2-p-methoxyphenylethyl)-5,6-dihydro-4H-1,3-oxazine 
• 4521-28-2 4-(4-Methoxyphenyl)butyric acid 
• 3153-44-4 4-(4-methoxy-phenyl)-4-oxo-butyric acid 
• 52244-70-9 4-(4-methoxyphenyl)butan-1-ol 

Downstream Products

• 1426580-95-1 1,7-bis-(3-iodo-4-methoxyphenyl)-heptan-3-one 
• 130233-83-9 1,7-bis(4'-hydroxyphenyl)-3-heptanone 
• 74185-15-2 1,7-bis(4-methoxyphenyl)heptan-3-ol 

Relevant articles and documents

Total synthesis of acerogenins E, G and K, and centrolobol

The first total synthesis of the diarylheptanoid acerogenins E and K, isolated from Acer nikoense MAXIM., is described. Formation of the 13-membered m,m-cyclophane skeleton was successfully achieved on the basis of a domino process involving a Miyaura arylborylation-intramolecular Suzuki reaction. The cyclization precursor was prepared via a Wittig reaction and Claisen-Schmidt condensation, which proceeded in moderate yields. The total synthesis of acerogenin G and centrolobol was also achieved from a common synthetic intermediate.