352352-20-6

Basic information

• Product Name: L-S-benzyl-β-homocysteine
• CAS NO: 352352-20-6
• Molecular Weight: 225.312
• Mol File: 352352-20-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-S-benzyl-β-homocysteine(CAS DataBase Reference)
• NIST Chemistry Reference: L-S-benzyl-β-homocysteine(352352-20-6)
• EPA Substance Registry System: L-S-benzyl-β-homocysteine(352352-20-6)

Safety Data

• Hazardous Substances Data: 352352-20-6(Hazardous Substances Data)

Upstream product

• 111639-20-4 (R)-4-benzylmercapto-3-phthalimido-butyric acid 
• 4378-12-5 (RS)-3-amino-4-benzylthiobutyric acid 
• 109566-36-1 S-benzyl-N,N-phthaloyl-L-cysteinyl chloride 

Relevant articles and documents

Capillary electrophoretic separation of enantiomers of amino acids and amino acid derivatives using crown ether and cyclodextrin

The capillary zone electrophoresis using (+)-18-crown-6-tetracarbonic acid as a chiral selector was a suitable method for the enantiomeric separation of racemates of amino acids and of some amino acid derivatives (esters, dipeptides). The influence of the chemical structure of the compounds on the separation was investigated. After optimization of the separation conditions, baseline separations were obtained for most racemates. The addition of acetonitrile and TBAB yielded an improvement of the separation. Improved selectivity was further observed by the application of a cyclodextrin, HP-β-CD, in combination with the crown ether.