922179-56-4

Basic information

• Product Name: (S)-7-(methoxymethoxy)-3-(4'-methoxymethoxy)-phenylchroman
• Synonyms: (S)-7-(methoxymethoxy)-3-(4'-methoxymethoxy)-phenylchroman
• CAS NO: 922179-56-4
• Molecular Weight: 330.381
• Mol File: 922179-56-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-7-(methoxymethoxy)-3-(4'-methoxymethoxy)-phenylchroman(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-7-(methoxymethoxy)-3-(4'-methoxymethoxy)-phenylchroman(922179-56-4)
• EPA Substance Registry System: (S)-7-(methoxymethoxy)-3-(4'-methoxymethoxy)-phenylchroman(922179-56-4)

Safety Data

• Hazardous Substances Data: 922179-56-4(Hazardous Substances Data)

Upstream product

• 922179-55-3 7-methoxymethoxy-3-(4'-methoxymethoxy-phenyl)-2H-chromen 
• 1236208-90-4 3-iodo-5,7-bis(methoxymethoxy)-4H-1-benzopyran-4-one 

Downstream Products

• 531-95-3 equol 

Relevant articles and documents

Enantioselective Total Synthesis of Natural Isoflavans: Asymmetric Transfer Hydrogenation/Deoxygenation of Isoflavanones with Dynamic Kinetic Resolution

A concise and highly enantioselective synthesis of structurally diverse isoflavans from a single chromone is described. The key transformation is a single-step conversion of racemic isoflavanones into virtually enantiopure isoflavans by domino asymmetric transfer hydrogenation/deoxygenation with dynamic kinetic resolution.