536730-54-8

Basic information

• Product Name: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N-(methoxymethyl)-, phenylmethyl ester
• CAS NO: 536730-54-8
• Molecular Formula: C23H29NO5
• Molecular Weight: 399.487
• Mol File: 536730-54-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N-(methoxymethyl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N-(methoxymethyl)-, phenylmethyl ester(536730-54-8)
• EPA Substance Registry System: L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N-(methoxymethyl)-, phenylmethyl ester(536730-54-8)

Safety Data

• Hazardous Substances Data: 536730-54-8(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 50-00-0 formaldehyd 
• 66617-58-1 N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 1376605-40-1 benzyl 4-benzyl-3-(methoxymethyl)-2-oxo-5-phenyloxazolidine-4-carboxylate 
• 536730-40-2 (2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenylpropionic acid 5-[(2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenyl-propionyloxy]-pentyl ester 
• 536730-39-9 (2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenylpropionic acid 4-[(2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenyl-propionyloxy]-butyl ester 
• 536730-55-9 (S)-N-tert-butoxycarbonyl-N-(methoxymethyl)-phenylalanine 2-(2-benzyloxyphenyl)ethyl ester 
• 432023-51-3 (S)-N-tert-butoxycarbonyl-N-(methoxymethyl)phenylalanine 2-(2-hydroxyphenyl)ethyl ester 
• 432023-52-4 (S)-N-tert-butoxycarbonyl-N-(methoxymethyl)phenylalanine 

Relevant articles and documents

Asymmetric intermolecular conjugate addition of amino acid derivatives via memory of chirality: Total synthesis of manzacidin A

Asymmetric intermolecular conjugate addition of α-amino acid derivatives with 4 via memory of chirality has been developed. The reactions proceeded in up to 98% ee with retention of configuration at the newly formed tetrasubstituted carbon center when R = Me. The product (R = Me) was transformed into manzacidin A.