168465-69-8

Basic information

• Product Name: (R)-α-(2-azidoethyl)benzenemethanol
• Synonyms: (R)-α-(2-azidoethyl)benzenemethanol
• CAS NO: 168465-69-8
• Molecular Weight: 177.206
• Mol File: 168465-69-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (R)-α-(2-azidoethyl)benzenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-α-(2-azidoethyl)benzenemethanol(168465-69-8)
• EPA Substance Registry System: (R)-α-(2-azidoethyl)benzenemethanol(168465-69-8)

Safety Data

• Hazardous Substances Data: 168465-69-8(Hazardous Substances Data)

Upstream product

• 113986-29-1 3-azido-1-phenyl-propan-1-one 
• 100306-33-0 (1R)-3-chloro-1-phenylpropanol 
• 127073-84-1 (R)-3-iodo-1-phenyl-1-propanol 

Downstream Products

• 240427-50-3 (3'R,5R)-5-tert-butyl-1-(3'-phenylhydroxypropyl)-hexahydro-2H-azepin-2-one 
• 1009805-60-0 7-(3-hydroxy-3-phenylpropyl)-7-azatricyclo[4.2.2.0^2,5]decan-8-one 
• 1009805-58-6 7-(3-hydroxy-3-phenylpropyl)-7-azatricyclo[4.2.2.0^2,5]decan-8-one 
• 357404-74-1 2-[[(1R)-3-azido-1-phenylpropyl]oxy]-4-chloro-5-fluorobenzonitrile 
• 357404-71-8 2-[[(1R)-3-azido-1-phenylpropyl]oxy]-4-chlorobenzonitrile 
• 357402-60-9 2-[[(1R)-3-amino-1-phenylpropyl]oxy]-4-chloro-5-fluorobenzonitrile 
• 357402-54-1 2-[[(1R)-3-amino-1-phenylpropyl]oxy]-4-chlorobenzonitrile 
• 570384-27-9 [4-(3-amino-1-phenyl-propoxy)-phenyl]-p-tolyl-methanone 
• 240427-47-8 (3'R,5R)-5-methyl-1-(3'-phenylhydroxypropyl)-hexahydro-2H-azepin-2-one 

Relevant articles and documents

A Green approach towards the synthesis of chiral alcohols using functionalized alginate immobilized Saccharomyces cerevisiae cells

The stereochemistry of the drug molecule is gaining greater therapeutic importance and thus much attention was drawn in synthesis of chiral compounds by the pharmaceutical industry. In this study Saccharomyces cerevisiae cells immobilized on functionalize

[3H]-(R)-NPTS, a radioligand for the type 1 glycine transporter.

The synthesis of NPTS, 6, a potent inhibitor of the type 1 glycine transporter (GlyT1) is described, as well as preparation of 6 in optically active and tritiated form for use as a radioligand for affinity displacement assay of GlyT1.

Novel use of phenylheteroakylamine derivatives

There is disclosed the use of a compound of formula (I) wherein R1, R2, X, Y, V, W and Z are as defined in the specification, and pharmaceutically acceptable salts, enantiomers or racemates thereof, in the manufacture of a medicament, for the treatment or prophylaxis of diseases or conditions in which inhibition of nitric oxide synthase activity is beneficial. Certain novel compounds of formula (Ia) and pharmaceutically acceptable salts thereof, and enantiomers and racemates thereof are disclosed; together with processes for their preparation, compositions containing them and their use in therapy. The compounds of formulae (I) and (Ia) are inhibitors of the enzyme nitric oxide synthase and are thereby particularly useful in the treatment or prophylaxis of inflammatory disease.