21931-02-2

Basic information

• Product Name: Carbamic acid, [(1S)-3-methyl-1-[(phenylamino)carbonyl]butyl]-, phenylmethyl ester
• CAS NO: 21931-02-2
• Molecular Formula: C20H24N2O3
• Molecular Weight: 340.422
• Mol File: 21931-02-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [(1S)-3-methyl-1-[(phenylamino)carbonyl]butyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(1S)-3-methyl-1-[(phenylamino)carbonyl]butyl]-, phenylmethyl ester(21931-02-2)
• EPA Substance Registry System: Carbamic acid, [(1S)-3-methyl-1-[(phenylamino)carbonyl]butyl]-, phenylmethyl ester(21931-02-2)

Safety Data

• Hazardous Substances Data: 21931-02-2(Hazardous Substances Data)

Upstream product

• 2018-66-8 Z-Leu-OH 
• 62-53-3 aniline 
• 2018-66-8 N-carbobenzyloxy leucine 
• 921-01-7 rac-cysteine 

Downstream Products

• 21930-99-4 N-benzoyl-L-leucine anilide 
• 21930-98-3 (S)-2-amino-4-methyl-N-phenylpentanamide 

Relevant articles and documents

MODULATORS OF SESTRIN-GATOR2 INTERACTION AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

Organocatalysis of asymmetric aldol reaction in water: Comparison of catalytic properties of (S)-valine and (S)-proline amides

(S)-Valine amides containing (S)- or (R)-α-phenylethyl substituents at N1 atom efficiently catalyze asymmetric aldol reactions between cyclic (heterocyclic) ketones and aromatic aldehydes in water, predominantly giving rise to the aldol anti-di

A novel generation of coupling reagents. Enantiodifferentiating coupling reagents prepared in situ from 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) and chiral tertiary amines

Coupling of racemic N-protected amino acids with amino components by means of 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) in the presence of chiral tertiary amines such as strychnine, brucine, and sparteine proceeds enantioselectively, affording appropriate amides or dipeptides in 69-85% yield. The configuration of the preferred enantiomer and enantiomeric enrichment depend on the structures of the amine and carboxylic acid. Calculated Kagan enantioselectivity parameters (s) are in the range 1.6-195. Chiral triazinylammonium chlorides formed in situ from CDMT and chiral tertiary amines are postulated as reactive intermediates involved in the process of enantioselective activation of N-protected amino acids.