250214-37-0

Basic information

• Product Name: Benzenepropanol, 5-broMo-g-phenyl-2-(phenylMethoxy)-, 4-Methylbenzenesulfonate (9CI)
• Synonyms: Benzenepropanol, 5-broMo-g-phenyl-2-(phenylMethoxy)-, 4-Methylbenzenesulfonate (9CI);3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropyl 4-methylbenzenesulfonate
• CAS NO: 250214-37-0
• Molecular Formula: C₂₉H₂₇BrO₄S
• Molecular Weight: 551.49128
• Mol File: 250214-37-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 675.9±55.0 °C(Predicted)
• Appearance: /
• Density: 1.337±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenepropanol, 5-broMo-g-phenyl-2-(phenylMethoxy)-, 4-Methylbenzenesulfonate (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, 5-broMo-g-phenyl-2-(phenylMethoxy)-, 4-Methylbenzenesulfonate (9CI)(250214-37-0)
• EPA Substance Registry System: Benzenepropanol, 5-broMo-g-phenyl-2-(phenylMethoxy)-, 4-Methylbenzenesulfonate (9CI)(250214-37-0)

Safety Data

• Hazardous Substances Data: 250214-37-0(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 621-82-9 Cinnamic acid 
• 1349883-68-6 (+/-)-4-bromo-2-(3-hydroxy-1-phenylpropyl)phenol 
• 156755-24-7 methyl 3-[2-(benzyloxy)-5-bromophenyl]-3-phenylpropanoate 
• 156755-23-6 6-bromo-4-phenyl-3,4-dihydro-2H-chromen-2-one 
• 106-41-2 4-bromo-phenol 
• 140-10-3 (E)-3-phenylacrylic acid 

Downstream Products

• 156755-35-0 methyl 4-(benzyloxy)-3-[(1R)-3-(dipropan-2-ylamino)-1-phenylpropyl]benzoate 
• 950773-38-3 R-(-)-[3-(2-benzyloxy-5-bromophenyl)-3-phenylpropyl]diisopropylamine 
• 207679-81-0 (R)-2-[3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)-phenol 
• 286930-02-7 fesoterodine 
• 286930-03-8 fesoterodine fumarate 
• 156755-37-2 {4-(benzyloxy)-3-[(1R)-3-(dipropan-2-ylamino)-1-phenylpropyl]phenyl}methanol 
• 156755-33-8 (R)-4-(benzyloxy)-3-(3-(diisopropylamino)-1-phenylpropyl)benzoic acid hydrochloride 
• 754159-68-7 4-(benzyloxy)-3-[(1R)-3-(dipropan-2-ylamino)-1-phenylpropyl]benzoic acid 
• 1135493-18-3 C₂₀H₁₈O₈*C₂₈H₃₄BrNO 
• 214601-12-4 (R)-N,N-diisopropyl-3-phenyl-3-(5-formyl-2-hydroxyphenyl)propyl-1-amine 
• 214601-16-8 (R)-(-)-3-(3-diisopropylamino-1-phenylpropyl)-4-hydroxybenzoic acid methyl ester 
• 194482-44-5 Tolterodine acid 
• 250214-44-9 2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxyl-methyl)phenyl isobutyrate 
• 837376-33-7 4-(benzyloxy)-3-(3-(diisopropylamino)-1-phenylpropyl)benzaldehyde 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF MUSCARINIC RECEPTOR ANTAGONIST

The present invention relates to novel and improved processes for the preparation of (r)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxymethyl)phenylisobutyrate represented by the following structural formula-1 and its pharmaceutically acceptable salts thereof.

PROCESS FOR PREPARATION OF PHENOLIC MONOESTERS OF HYDROXYMETHYL PHENOLS

Disclosed herein is an improved and efficient process for preparation of fesoterodine and its pharmaceutically acceptable salt. Disclosed also herein is novel intermediate of formula (III). Also disclosed are metal salts of formula (XII) and preparation thereof.

IMPROVED PROCESS FOR DIPHENYLPROPYLAMINE DERIVATIVES

The present invention relates to an improved process for the preparation of biologically active diphenylpropylamine derivatives. The present invention specifically relates to an improved fesoterodine of formula (I) and its pharmaceutically acceptable salts.