120349-74-8

Basic information

• Product Name: METHYL (2R)-2-AMINO-3-(4-METHOXYPHENYL)PROPANOATE
• Synonyms: METHYL (2R)-2-AMINO-3-(4-METHOXYPHENYL)PROPANOATE;O-Methyl-D-tyrosine methyl ester
• CAS NO: 120349-74-8
• Molecular Formula: C₁₁H₁₅NO₃
• Molecular Weight: 209.24
• Mol File: 120349-74-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: METHYL (2R)-2-AMINO-3-(4-METHOXYPHENYL)PROPANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL (2R)-2-AMINO-3-(4-METHOXYPHENYL)PROPANOATE(120349-74-8)
• EPA Substance Registry System: METHYL (2R)-2-AMINO-3-(4-METHOXYPHENYL)PROPANOATE(120349-74-8)

Safety Data

• Hazardous Substances Data: 120349-74-8(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 39878-65-4 (R)-β-(4-methoxyphenyl)alanine 
• 3728-20-9 D-tyrosine methylester hydrochloride 
• 556-02-5 tyrosine 
• 76757-90-9 N-(tert-butoxycarbonyl)-D-tyrosine methyl ester 
• 94790-24-6 (2R)-tert-butoxycarbonylamino-3-(4-methoxyphenyl)propionic acid methyl ester 
• 70601-63-7 (D)-4-methoxyphenylalanine hydrochloride 

Downstream Products

• 1225439-14-4 methyl (R)-2-(3-1H-imidazol-4-ylpropionyl-amino)-3-(4-methoxyphenyl)propanoate 
• 120349-77-1 (Z)-(R)-4-tert-Butoxycarbonylamino-5-(4-methoxy-phenyl)-pent-2-enoic acid methyl ester 
• 120349-78-2 [(Z)-(R)-4-Hydroxy-1-(4-methoxy-benzyl)-but-2-enyl]-carbamic acid tert-butyl ester 
• 120349-75-9 (2R)-2-(tert-butoxycarbonyl)amino-3-(4-methoxyphenyl)propan-1-ol 
• 120349-79-3 (R)-2-(4-Methoxy-benzyl)-2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester 
• 139183-60-1 [(R)-1-Formyl-2-(4-methoxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 21399-39-3 (R)-2-(p-methoxyphenyl)methy-2,5-dihydropyrrole 
• 400009-30-5 (2S,3S,4R)-benzyloxy-4-N,N-dibenzylamino-3-hydroxy-5-(4'-methoxy-phenyl)pentan-1-ol 
• 400009-28-1 (R)-2-Dibenzylamino-3-(4-methoxy-phenyl)-propan-1-ol 
• 400009-27-0 (R)-2-Dibenzylamino-3-(4-methoxy-phenyl)-propionaldehyde 
• 733769-83-0 (S)-2-{3-[(R)-2-Acryloylamino-3-(4-methoxy-phenyl)-propionylamino]-propionyloxy}-4-methyl-pentanoic acid (S)-1-[(S)-1-((2R,3R)-3-phenyl-oxiranyl)-ethyl]-but-3-enyl ester 
• 733769-90-9 (S)-2-{3-[(R)-2-Acryloylamino-3-(4-methoxy-phenyl)-propionylamino]-propionyloxy}-4-methyl-pentanoic acid tert-butyl ester 
• 1026015-46-2 (S)-2-{3-[(R)-2-Acryloylamino-3-(4-methoxy-phenyl)-propionylamino]-propionyloxy}-4-methyl-pentanoic acid 
• 1027261-48-8 3-[(R)-2-Acryloylamino-3-(4-methoxy-phenyl)-propionylamino]-propionic acid ethyl ester 

Relevant articles and documents

OXOAZETIDINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND USE THEREOF IN HUMAN MEDICINE AND IN COSMETICS

The present invention relates to novel compounds derived from oxoazetidine corresponding to general formula (I) to the compositions containing same, to the process for preparation thereof and to the use thereof in pharmaceutical or cosmetic compositions.

An aldol-based approach to the synthesis of the antibiotic anisomycin

Chemical equation presented A new approach to the synthesis of the antibiotic anisomycin is reported that relies upon a key aldol disconnection. The glycolate aldol coupling proceeds in 75% yield and with >95% diastereoselectivity, which allows the 13-step synthesis to proceed in 35% overall yield.