88950-54-3

Basic information

• Product Name: 2-Propenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (4-nitrophenyl)methyl ester
• Synonyms: 4-nitrobenzyl 2-[(tert-butoxycarbonyl)amino]acrylate;N-Boc-dehydroalanine p-nitrobenzyl ester
• CAS NO: 88950-54-3
• Molecular Formula: C15H18N2O6
• Molecular Weight: 322.318
• Mol File: 88950-54-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (4-nitrophenyl)methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (4-nitrophenyl)methyl ester(88950-54-3)
• EPA Substance Registry System: 2-Propenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (4-nitrophenyl)methyl ester(88950-54-3)

Safety Data

• Hazardous Substances Data: 88950-54-3(Hazardous Substances Data)

Upstream product

• 123311-11-5 4-nitrobenzyl 2-[(tert-butoxycarbonyl)amino]-3-hydroxypropanoate 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 3850-40-6 N-Boc-DL-serine 

Downstream Products

• 123311-13-7 N-Boc-3-amino-3-(4-nitrobenzyloxycarbonyl)-5,5-dimethyl-1-pyrazoline 
• 88950-63-4 (1S,2R)-1-tert-Butoxycarbonylamino-2-isopropyl-cyclopropanecarboxylic acid 4-nitro-benzyl ester 
• 88950-62-3 (1S,2S)-1-tert-Butoxycarbonylamino-2-ethyl-cyclopropanecarboxylic acid 4-nitro-benzyl ester 
• 88950-61-2 (1S,2S)-1-tert-Butoxycarbonylamino-2-methyl-cyclopropanecarboxylic acid 4-nitro-benzyl ester 
• 88950-60-1 1-tert-Butoxycarbonylamino-cyclopropanecarboxylic acid 4-nitro-benzyl ester 
• 88950-68-9 (1RS,2SR)-1-[(tert-butoxycarbonyl)amino]-2-phenylcyclopropane-1-carboxylic acid 
• 88950-65-6 (1R,2R)-1-tert-Butoxycarbonylamino-2-methyl-cyclopropanecarboxylic acid 
• 88950-64-5 1-<(tert-butyloxy)carbonylamino>cyclopropane-1-carboxylic acid 
• 123311-15-9 N-Boc-2,3-methanovaline p-nitrobenzyl ester 
• 686744-30-9 N,N-di-(tert-butoxycarbonyl)-dehydroalanine p-nitrobenzyl ester 

Relevant articles and documents

Efficient synthesis of protected cyclopropyl β-aspartylphosphates

The in situ reaction of protected dehydroamino acids with derivatives of vinyldiazomethane leads to good to excellent yields of vinyl cyclopropanes via 3 + 2 dipolar cycloaddition followed by N2 extrusion. Chromatographic separation of the cycl

Synthesis of (±)-2,3-methanovaline and (±)-2,3- methanoleucine

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