64896-37-3

Basic information

• Product Name: (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate
• Synonyms: (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate
• CAS NO: 64896-37-3
• Molecular Formula: C₁₁H₂₁NO₄
• Molecular Weight: 231.28874
• Mol File: 64896-37-3.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate(64896-37-3)
• EPA Substance Registry System: (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate(64896-37-3)

Safety Data

• Hazardous Substances Data: 64896-37-3(Hazardous Substances Data)

Usage

Description

(S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate is a chiral compound that features a methyl group, a pentanoate chain, and a protected amine group. It is characterized by its specific stereochemistry, with the "S" configuration indicating the spatial arrangement of its atoms. (S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate is of interest in the field of organic chemistry and pharmaceuticals due to its potential applications in the synthesis of various biologically active molecules.

Uses

Used in Pharmaceutical Industry:
(S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex molecular structures. Its protected amine group allows for selective reactions, making it a valuable building block in the development of new drugs.
Used in Antiviral Applications:
(S)-Methyl 2-((tert-butoxycarbonyl)aMino)pentanoate is used as a potential antiviral agent for preventing or treating infections caused by Pneumovirinae viruses. Its specific structure may interact with viral components or host cell receptors, thereby inhibiting viral replication or attachment, which can help in managing or preventing such infections.

Upstream product

• 811-49-4 ethyllithium 
• 93267-04-0 N-(tert-butoxycarbonyl)-L-3-iodoalanine methyl ester 
• 917-54-4 methyllithium 
• 76969-87-4 tert-Butyloxycarbonyl-L-α-amino-γ-bromobutyric acid methyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 56558-30-6 methyl L-norvalinate hydrochloride 
• 142729-70-2 D,L-N-Boc-nor-valine methyl ester 
• 162007-08-1 methyl (2S)-(tert-butoxycarbonylamino)-5-iodopentanoate 
• 107-05-1 3-chloroprop-1-ene 
• 1239606-51-9 tert-butyl (S)-1-(methoxycarbonyl)buta-2,3-dienylcarbamate 
• 101650-17-3 (S)-2-amino-4-bromobutyric acid methyl ester 
• 56926-94-4 methyl (2S)-2-[N-(t-butoxycarbonyl)amino]-3-(4-methylbenzenesulfonyl)-oxypropionate 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 186581-53-3 diazomethane 

Downstream Products

• 160801-74-1 (2S)-2-(1,1-dimethylethoxycarbonylamino)pentanal 
• 1158971-62-0 1,1-dimethylethyl {(1S)-1-[bis(4-fluorophenyl)(hydroxy)methyl]butyl}carbamate 

Relevant articles and documents

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Oxazolidinones and 2,5-Dihydrofurans via Zinc-Catalyzed Regioselective Allenylation Reactions of l -α-Amino Aldehydes

The simultaneous control of diastereoselectivity and regioselectivity in Zn-catalyzed allenylation reactions of N-protected l-α-amino aldehydes is reported. A reversal in diastereoselectivity could be realized by variation of the α-amino aldehyde protecti

Synthesis of optically active α-(allenyl)-and a-substituted-α- (allenyl)glycines

The synthesis of various types of optically active α-(allenylsilane- containing)glycines via a chiralitytransferring ester-enolate Claisen rearrangement of α-acyloxy-a-alkynylsilanes is described. The conversion of the rearranged products into the optically active silicon-free α-(allenyl)-and α-substituted-α-(allenyl)glycines was achieved by the removal of the Me2PhSi-or TMS group from the allene terminus.