953393-41-4

Basic information

• Product Name: [(S)-1-(Anthracen-1-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester
• Synonyms: [(S)-1-(Anthracen-1-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester
• CAS NO: 953393-41-4
• Molecular Weight: 474.559
• Mol File: 953393-41-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [(S)-1-(Anthracen-1-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(S)-1-(Anthracen-1-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(953393-41-4)
• EPA Substance Registry System: [(S)-1-(Anthracen-1-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester(953393-41-4)

Safety Data

• Hazardous Substances Data: 953393-41-4(Hazardous Substances Data)

Upstream product

• 1161-13-3 N-Cbz-L-Phe 
• 3397-32-8 N-(benzyloxycarbonyl)-phenylalanine-N-hydroxysuccinimide ester 
• 610-49-1 1-aminoanthracene 

Downstream Products

• 615580-71-7 (S)-2-amino-N-(anthracene-1-yl)-3-phenylpropan-amide 

Relevant articles and documents

A turn-on fluorescent indicator for citrate with micromolar sensitivity

A turn-on fluorescent indicator for citric acid (citrate) has been developed, displaying high emission enhancement (+1500%) and low interference by other carboxylates. The sensor is based on the non-emissive copper(ii) complex of a fluorescent amino amide, which, upon addition of citrate decomplexates to yield the emissive ligand. The detection limit estimated for this new chemosensing system is about 0.5 M. This novel approach to the analysis of citrate constitutes an alternative ca. 102-103 times more sensitive than the standard method based on the enzyme citrate lyase. The Royal Society of Chemistry.

Nickel complexes from α-amino amides as efficient catalysts for the enantioselective Et2Zn addition to benzaldehyde

Ni2+ complexes derived from simple α-amino amides catalyze very efficiently the addition of Et2Zn to benzaldehyde, giving (S)-1-phenylethanol as the major isomer in most cases (94% yield, 97% ee for R=Bn). The nature of the substituent on the amide nitrogen atom seems to play a key role in determining the asymmetric induction observed.