112670-44-7

Basic information

• Product Name: Carbamic acid, [2-(butylamino)-2-oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (S)-
• CAS NO: 112670-44-7
• Molecular Formula: C18H28N2O3
• Molecular Weight: 320.432
• Mol File: 112670-44-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(butylamino)-2-oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(butylamino)-2-oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (S)-(112670-44-7)
• EPA Substance Registry System: Carbamic acid, [2-(butylamino)-2-oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (S)-(112670-44-7)

Safety Data

• Hazardous Substances Data: 112670-44-7(Hazardous Substances Data)

Upstream product

• 66617-58-1 N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester 
• 109-73-9 N-butylamine 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 

Downstream Products

• 264887-19-6 H₂N-L-Val-L-Phe-Bu 
• 329324-40-5 [(S)-1-((S)-1-Butylcarbamoyl-2-phenyl-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid tert-butyl ester 
• 329324-39-2 N-[(2-hydroxyphenyl)methylene]-L-valyl-N-butyl-L-phenylalaninamide 
• 896105-74-1 Boc-L-Tle-L-Phe-NHBu 
• 896105-75-2 L-Tle-L-Phe-NHBu 
• 1236254-97-9 L-Phe-NHBu*HCl 

Relevant articles and documents

Enantioselective synthesis of arylamines through Zr-catalyzed addition of dialkylzincs to imines. Reaction development by screening of parallel libraries [5]

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Synthesis of highly substituted imidazolidine-2,4-dione (Hydantoin) through Tf2O-mediated dual activation of Boc-protected dipeptidyl compounds

Highly substituted chiral hydantoins were readily synthesized from simple dipeptides in a single step under mild conditions. This reaction proceeded through the dual activation of an amide and a tert-butyloxycarbonyl (Boc) protecting group by Tf2O-pyridine. This method was successfully applied in the preparation of a variety of biologically active compounds, including drug analogs and natural products.

A chiral Ag-based catalyst for practical, efficient, and highly enantioselective additions of enolsilanes to α-ketoesters

A Ag-based chiral catalyst promotes efficient and highly enantioselective aldol additions of ketone-derived enolsilanes to α-ketoesters in the presence of a readily available amino acid-based ligand and commercially available AgF2. α-Ketoester