1255212-57-7

Basic information

• Product Name: (1R,2S)-1-phenyl-2-(N,2,4,6-tetramethylphenylsulfonamido)propyl (2R,3S)-4-(tert-butoxycarbonyl(methyl)amino)-3-hydroxy-2-methylbutanoate
• Synonyms: (1R,2S)-1-phenyl-2-(N,2,4,6-tetramethylphenylsulfonamido)propyl (2R,3S)-4-(tert-butoxycarbonyl(methyl)amino)-3-hydroxy-2-methylbutanoate
• CAS NO: 1255212-57-7
• Molecular Weight: 576.755
• Mol File: 1255212-57-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2S)-1-phenyl-2-(N,2,4,6-tetramethylphenylsulfonamido)propyl (2R,3S)-4-(tert-butoxycarbonyl(methyl)amino)-3-hydroxy-2-methylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-1-phenyl-2-(N,2,4,6-tetramethylphenylsulfonamido)propyl (2R,3S)-4-(tert-butoxycarbonyl(methyl)amino)-3-hydroxy-2-methylbutanoate(1255212-57-7)
• EPA Substance Registry System: (1R,2S)-1-phenyl-2-(N,2,4,6-tetramethylphenylsulfonamido)propyl (2R,3S)-4-(tert-butoxycarbonyl(methyl)amino)-3-hydroxy-2-methylbutanoate(1255212-57-7)

Safety Data

• Hazardous Substances Data: 1255212-57-7(Hazardous Substances Data)

Upstream product

• 123387-72-4 O-tert-butyl N-methyl-N-(2-oxoethyl)carbamate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 57561-39-4 methyl(2-hydroxyethyl)carbamic acid tert-butyl ester 

Downstream Products

• 1255213-14-9 C₂₉H₄₅N₅O₆ 
• 1255213-10-5 C₂₉H₄₅N₅O₆ 
• 1255213-06-9 C₂₆H₄₃N₅O₆ 
• 1255213-03-6 C₃₀H₄₁N₃O₈ 
• 1255213-02-5 C₃₀H₄₁N₃O₈ 
• 1255212-99-7 C₂₉H₃₉N₃O₈ 
• 1255212-98-6 C₂₉H₃₉N₃O₈ 
• 1255212-95-3 C₃₆H₅₆FN₃O₈Si 
• 1255212-94-2 C₃₆H₅₆FN₃O₈Si 
• 1255212-86-2 (2S,5S,6S)-tert-Butyl 2-(tert-butyldimethylsilyloxy)-4-(1-(4-methoxybenzyloxy)propan-2-ylamino)-3-methylbutyl(methyl)carbamate 
• 1255212-84-0 (2R,5S,6S)-tert-Butyl 2-(tert-butyldimethylsilyloxy)-4-(1-(4-methoxybenzyloxy)propan-2-ylamino)-3-methylbutyl(methyl)carbamate 
• 1255212-78-2 (2S,5R,6S)-tert-butyl-2-(tert-butyldimethylsilyloxy)-4-(1-(4-methoxybenzyloxy)propan-2-ylamino)-3-methyl-4-oxobutyl(methyl)carbamate 
• 1255212-76-0 (2R,5S,6S)-tert-butyl-2-(tert-butyldimethylsilyloxy)-4-(1-(4-methoxybenzyloxy)propan-2-ylamino)-3-methyl-4-oxobutyl(methyl)carbamate 
• 1255213-87-6 C₄₉H₅₉N₃O₉ 

Relevant articles and documents

Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions

Orthogonally protected chiral β-hydroxy-γ-amino acids can be accessed in >100 g quantities from readily available starting materials and reagents in three to four steps. These chiral synthons contain two adjacent stereocenters along with suitably protecte