85803-44-7

Basic information

• Product Name: (S)-2-AMINO-3-[4-(PHENYLMETHOXY)PHENYL]-1-PROPANOL
• Synonyms: TYROSINOL(BENZYL);(S)-2-AMINO-3-[4-(PHENYLMETHOXY)PHENYL]-1-PROPANOL;O-BENZYL-L-TYROSINOL;H-TYR(BZL)-OL;H-TYROSINOL(BZL);L-TYROSINOL(BENZYL);L-Tyr(Bzl)-ol;(S)-2-Amino-3-(4-(benzyloxy)phenyl)propan-1-ol
• CAS NO: 85803-44-7
• Molecular Formula: C₁₆H₁₉NO₂
• Molecular Weight: 257.33
• Mol File: 85803-44-7.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0-5°C
• CAS DataBase Reference: (S)-2-AMINO-3-[4-(PHENYLMETHOXY)PHENYL]-1-PROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-AMINO-3-[4-(PHENYLMETHOXY)PHENYL]-1-PROPANOL(85803-44-7)
• EPA Substance Registry System: (S)-2-AMINO-3-[4-(PHENYLMETHOXY)PHENYL]-1-PROPANOL(85803-44-7)

Safety Data

• Hazardous Substances Data: 85803-44-7(Hazardous Substances Data)

Usage

Chemical Properties

White solid

Upstream product

• 16652-64-5 O-benzyl-S-tyrosine 
• 34805-17-9 methyl 2S-amino-3-(4-benzyloxyphenyl)propionate hydrochloride 
• 66605-58-1 O-benzyl N-Boc-L-tyrosinol 
• 1080-06-4 L-Tyr-OMe 
• 27513-44-6 N-tert-butoxycarbonyl-O-benzyl-(S)-tyrosine methyl ester 
• 4326-36-7 (S)-N-(tert-butoxycarbonyl)tyrosine methyl ester 
• 60-18-4 L-tyrosine 
• 2130-96-3 O-benzyl-N-tert-butoxycarbonyl-L-tyrosine 
• 100-39-0 benzyl bromide 
• 110-91-8 morpholine 
• 541-41-3 chloroformic acid ethyl ester 
• 72594-77-5 N-(tert-butoxycarbonyl)-L-tyrosine ethyl ester 
• 127132-32-5 ethyl N-{[(1,1-dimethylethyl)oxy]carbonyl}-O-(phenylmethyl)-L-tyrosinate 
• 5034-68-4 4-[(2S)-2-amino-3-hydroxypropyl]phenol 

Downstream Products

• 132376-98-8 (4S)-4-(4'-benzyloxy)benzyl-4,5-dihydrooxazoline 
• 183794-24-3 (S)-1-(4-Benzyloxy-benzyl)-2-[(Z)-4-(tert-butyl-dimethyl-silanyloxy)-but-2-enyloxy]-ethylamine 
• 170438-03-6 (S)-4-(4-(benzyloxy)benzyl)oxazolidin-2-one 
• 600738-28-1 N₁,N₃-di{(1S)-1-[4-(benzyloxy)benzyl]-2-hydroxyethyl}-2,2-diethylmanonamide 
• 842977-86-0 (S,S)-N,N'-bis{1-[4-(benzyloxy)benzyl]-2-hydroxyethyl}ethanediamide 
• 870450-03-6 6-[(S)-2-(4-Benzyloxy-phenyl)-1-hydroxymethyl-ethylcarbamoyl]-nicotinic acid methyl ester 
• 848828-71-7 (S)-2-azido-3-(4-benzyloxyphenyl)propan-1-ol 
• 888494-17-5 {benzyl-[2-(4-benzyloxy-phenyl)-1-hydroxymethyl-ethyl]-amino}-acetic acid tert-butyl ester 
• 870450-04-7 6-[(S)-2-(4-Benzyloxy-phenyl)-1-methanesulfonyloxymethyl-ethylcarbamoyl]-nicotinic acid methyl ester 
• 842977-93-9 (S,S)-N,N'-bis[2-hydroxy-1-(4-hydroxybenzyl)ethyl]ethanediamide 
• 468732-54-9 2,2'-(1-ethylpropylidene)bis[(4S)-4-(4-benzyloxy)benzyl-4,5-dihydro-1,3-oxazole] 
• 600738-30-5 N₁,N₃-di{(1S)-1-[4-(benzyloxy)benzyl]-2-chloroethyl}-2,2-diethylmanonamide 
• 444753-23-5 (5S)-5-[4-(benzyloxy)benzyl]-4-(tert-butoxycarbonyl)morpholin-3-one 
• 444753-30-4 (2S,5S)-2-benzyl-4-(tert-butoxycarbonyl)-5-(4-hydroxybenzyl)morpholin-3-one 

Relevant articles and documents

N-[4-phenyl-3-(benzoylamino)-1,1,1-trifluoro-butyl-2-yl]-phenylalaninol derivative as well as preparation method and application thereof

The present invention discloses an N-[4-phenyl-3-(benzoylamino)-1,1,1-trifluoro-butyl-2-yl]-phenylalaninol derivative, which is a compound represented by a general formula I and a pharmaceutically acceptable salt or hydrate thereof, and wherein R1 and R3

Soluble polymer supported 2-imidazolidinone chiral auxiliary and method for manufacturing the same

The present invention relates to a chiral auxiliary agent and a manufacturing method thereof and, more specifically, to a 2-imidazolidinone chiral auxiliary agent supported onto a polymer soluble in an organic solvent and a manufacturing method thereof. The chiral auxiliary agent in the present invention shows effects of being easy to separate reaction products and the chiral auxiliary agent after a termination of a reaction while fulfilling an economic efficacy of chiral auxiliary molecules by being supported onto the polymer soluble in the organic solvent.COPYRIGHT KIPO 2015

New practical synthesis of non-cross-linked polystyrene supported 2-phenylimino-2-oxazolidine

A new practical method for the synthesis of a non-cross-linked polystyrene supported 2-phenylimino-2-oxazolidine chiral auxiliary is reported. This method started from the same material as in a previous synthesis, N-Boc-L-tyrosine ethyl ester, but the overall yield was 42.5%, which was higher than the copolymerisation method.