131791-82-7

Basic information

• Product Name: methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate
• Synonyms: methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate
• CAS NO: 131791-82-7
• Molecular Weight: 209.245
• Mol File: 131791-82-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate(131791-82-7)
• EPA Substance Registry System: methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate(131791-82-7)

Safety Data

• Hazardous Substances Data: 131791-82-7(Hazardous Substances Data)

Upstream product

• 309977-86-4 (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-methoxyphenyl)propanoate 
• 79-20-9 acetic acid methyl ester 
• 123-11-5 4-methoxy-benzaldehyde 
• 329013-12-9 (S)-N-tert-butyloxycarbonyl β-Tyr 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 1271792-72-3 (R,Z)-methyl 3-(4-methoxyphenyl)-3-(1-phenylethylamino)acrylate 
• 131791-82-7 3-amino-3-(4-methoxyphenyl)propionic acid methyl ester 
• 5678-45-5 3-amino-3-(4-methoxyphenyl)propionic acid 
• 22027-50-5 methyl 3-(4-methoxybenzoyl)acetate 
• 67-56-1 methanol 
• 131791-83-8 (S)-2-tert-Butyl-6-(4-methoxyphenyl)-5,6-dihydro-4-(1H)-pyrimidinone 

Downstream Products

• 131791-80-5 N-Boc-(S)-alanyl-N-methyl-2-bromo-(R)-tryptophanyl-O-methyl-(R)-β-tyrosine Methyl Ester 
• 159848-76-7 methyl (+)-(3S)-3-amino-3-(4-methoxyphenyl)propanoate 
• 131791-82-7 methyl (-)-(3R)-3-amino-3-(4-methoxyphenyl)propanoate 
• 1246195-54-9 C₁₄H₁₉NO₅ 
• 131690-56-7 (S)-β-amino-β-(4-methoxyphenyl)propionic acid 
• 1243990-40-0 C₃₀H₃₉N₃O₇ 
• 1218781-43-1 C₂₂H₃₄N₂O₆ 
• 1218781-44-2 C₁₇H₂₆N₂O₄ 
• 1218781-47-5 C₃₃H₅₃N₅O₆ 
• 96363-21-2 methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate 

Relevant articles and documents

Catalytic asymmetric oxidative carbonylation-induced kinetic resolution of sterically hindered benzylamines to chiral isoindolinones

A highly enantioselective kinetic resolution of sterically hindered benzylamines has been achieved for the first time through transition-metal-catalyzed oxidative carbonylation, in which the new KR strategy offered a new approach to afford chiral isoindolinones (er up to 97?:?3) and the origin of chemoselectivity and stereoselectivity was confirmed by density functional theory (DFT) calculations.

Effect of the 4′-substituted phenylalanine moiety of sansalvamide A peptide on antitumor activity

Eight sansalvamide A peptide analogues with 4′-fluoride, 4′-chloride, 4′-bromide, 4′-iodide, and 4′- methoxyphenylalanine moieties were synthesized. The effect of these para-substitutions of sansalvamide A peptide on their cytotoxicity was evaluated using HCT-116, MDA-MB-231, HT-29, HCT-15, K562, HeLa, and A549 cell lines. The 4′-methoxyphenylalanine analog of sansalvamide A peptide was found to be a promising antitumor agent.

Synthesis and biological evaluation of new jasplakinolide (jaspamide) analogs

Synthesis and biological evaluation of jasplakinolide analogs are described. The synthesis of analogs utilized a diastereoselective syn-aldol reaction and an orthoester Claisen rearrangement as key steps. All synthetic analogs were evaluated for their abi