115424-05-0

Basic information

• Product Name: Carbamic acid, [2-hydroxy-1-[(4-methoxyphenyl)methyl]ethyl]-, phenylmethyl ester, (S)-
• CAS NO: 115424-05-0
• Molecular Formula: C18H21NO4
• Molecular Weight: 315.369
• Mol File: 115424-05-0.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-hydroxy-1-[(4-methoxyphenyl)methyl]ethyl]-, phenylmethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-hydroxy-1-[(4-methoxyphenyl)methyl]ethyl]-, phenylmethyl ester, (S)-(115424-05-0)
• EPA Substance Registry System: Carbamic acid, [2-hydroxy-1-[(4-methoxyphenyl)methyl]ethyl]-, phenylmethyl ester, (S)-(115424-05-0)

Safety Data

• Hazardous Substances Data: 115424-05-0(Hazardous Substances Data)

Upstream product

• 121778-71-0 (S)-2-(benzyloxycarbonylamino)-3-(4-methoxyphenyl)-1-propionic acid methyl ester 
• 6230-11-1 O-Methyltyrosine 
• 17355-19-0 methyl (S)-2-amino-3-(4-methoxyphenyl)propionate 
• 1164-16-5 Z-L-Tyr-OH 
• 53796-61-5 N-acetyl-O-methyl-tyrosine 
• 6330-11-6 O-methyl-L-tyrosine ethyl ester; hydrochloride 
• 137960-06-6 (R)-4-(4-Hydroxy-benzoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 16679-94-0 N-[(phenylmethoxy)carbonyl]-L-tyrosine 
• 949-67-7 L-tyrosine ethyl ester 
• 501-53-1 benzyl chloroformate 
• 7479-01-8 O-methyl-L-tyrosine methyl ester hydrochloride 
• 60-18-4 L-tyrosine 
• 17554-34-6 (2S)-2-[(benzyloxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid 
• 3417-91-2 L-tyrosine methyl ester HCl 

Downstream Products

• 209266-21-7 N-(benzyloxycarbonyl)-O-methyl-L-tyrosinal 
• 20989-19-9 (2S)-2-amino-3-(4-methoxyphenyl)propan-1-ol 
• 115424-09-4 N-Cbz-2-(4-methoxyphenyl)-1-methylethylamine 
• 115424-07-2 [(S)-1-Iodomethyl-2-(4-methoxy-phenyl)-ethyl]-carbamic acid benzyl ester 
• 621-84-1 O-benzyl carbamate 
• 140-67-0 Estragole 
• 611210-10-7 N-((1S)-1-(2,5-dioxolanyl)-2-(4-methoxyphenyl)ethyl)(benzyloxy)formamide 
• 611210-38-9 (2S)-N-[(1S)-1-(1,3-dioxolan-2-yl)-2-(4-methoxyphenyl)ethyl]-2-hydroxy-4-methylpentanamide 
• 611210-22-1 (1S)-1-(1,3-dioxolan-2-yl)-2-(4-methoxyphenyl)ethanamine 
• 115424-06-1 Toluene-4-sulfonic acid (S)-2-benzyloxycarbonylamino-3-(4-methoxy-phenyl)-propyl ester 
• 17554-34-6 (2S)-2-[(benzyloxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid 

Relevant articles and documents

Synthesis of Water-Soluble Chiral DOTA Lanthanide Complexes with Predominantly Twisted Square Antiprism Isomers and Circularly Polarized Luminescence

One-step cyclization of a tetraazamacrocycle 5 with 70% yield in a 25-g scale was performed. Its chiral DOTA derivatives, L4, has ?93% of TSAP coordination isomer in its Eu(III) and Yb(III) complexes in aqueous solution. [GdL4]5- exhibits a high relaxivity, making it a promising and efficient MRI contrast agent. High luminescence dissymmetry factor (glum) values of 0.285 (ΔJ = 1) for [TbL3]- and 0.241 (ΔJ = 1) for [TbL4]5- in buffer solutions were recorded.

Asymmetric synthesis of unnatural amino acids and tamsulosin chiral intermediate

An efficient and enantioselective hydrogenation of N-acetylamino phenyl acrylic acids was successfully developed by using ruthenium catalyst. This methodology is important in the field of pharmaceuticals and provides a new process for the preparation of unnatural amino acids and tamsulosin chiral intermediate.

HYDROXYMORPHOLINONE DERIVATIVE AND MEDICINAL USE THEREOF

A compound represented by the following formula (I) wherein R1 and R2 are each a lower alkyl group optionally having substituents, which has a calpain inhibitory activity, or a salt thereof is provided.