907192-58-9

Basic information

• Product Name: Phenol, 3-[[[3-(4-methoxyphenoxy)propyl]amino]methyl]-
• CAS NO: 907192-58-9
• Molecular Formula: C17H21NO3
• Molecular Weight: 287.359
• Mol File: 907192-58-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 3-[[[3-(4-methoxyphenoxy)propyl]amino]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-[[[3-(4-methoxyphenoxy)propyl]amino]methyl]-(907192-58-9)
• EPA Substance Registry System: Phenol, 3-[[[3-(4-methoxyphenoxy)propyl]amino]methyl]-(907192-58-9)

Safety Data

• Hazardous Substances Data: 907192-58-9(Hazardous Substances Data)

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 
• 100841-00-7 3-(4-methoxyphenoxy)propan-1-amine 

Downstream Products

• 848260-89-9 3-({benzoxazol-2-yl[3-(4-methoxyphenoxy)propyl]amino}methyl)phenol 

Relevant articles and documents

Enantioselective synthesis of the PPARα agonist (R)-K-13675 via (S)-2-hydroxybutyrolactone

Enantioselective synthesis of enantiomerically pure PPARα agonist (R)-K-13675 can be achieved starting from (S)-2-hydroxybutyrolactone. An important intermediate, 2-(aryloxy)butyrolactone, was prepared by reaction of the phenol with (S)-2-hydroxybutyrolactone in excellent yield without loss of enantiomeric purity using the Mitsunobu reaction, followed by conversion into the 2-(aryloxy)butanoic acid via the 2-(aryloxy)-4-iodobutanoate by cleavage of the lactone on exposure to iodotrimethylsilane, followed by hydrogenolysis and hydrolysis. Georg Thieme Verlag Stuttgart.

PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE PPAR-ACTIVATING COMPOUND AND INTERMEDIATE OF THE SAME

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