5661-10-9

Basic information

• Product Name: 5,6-Dihydro-4H-cyclopenta[d][1,3]thiazole
• Synonyms: 5,6-Dihydro-4H-cyclopenta[d][1,3]thiazole;4H,5H,6H-cyclopenta[d][1,3]thiazole
• CAS NO: 5661-10-9
• Molecular Formula: C6H7NS
• Molecular Weight: 125.19148
• Mol File: 5661-10-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 80 °C(Press: 11 Torr)
• Appearance: /
• Density: 1.236±0.06 g/cm3(Predicted)
• PKA: 3.69±0.20(Predicted)
• CAS DataBase Reference: 5,6-Dihydro-4H-cyclopenta[d][1,3]thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-Dihydro-4H-cyclopenta[d][1,3]thiazole(5661-10-9)
• EPA Substance Registry System: 5,6-Dihydro-4H-cyclopenta[d][1,3]thiazole(5661-10-9)

Safety Data

• Hazardous Substances Data: 5661-10-9(Hazardous Substances Data)

Upstream product

• 694-28-0 2-chlorocyclopentanone 
• 60-29-7 diethyl ether 
• 115-08-2 thiocarboxamide 

Relevant articles and documents

Process for the preparation of chiral keto-heterocycles of basic amino acids

A process for the preparation of novel keto heterocycle derivatives of basic natural and unnatural amino acids which affords products of high enantiomeric excess where a metalated heterocycle is reacted with N,O-dialkyl amide of an amino acid containing arylsulphonamide protected side chain amine in high chemical and optical yield as well as the novel compounds obtained by the process.

New N-aryl and N-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme A: cholesterol acyl transferase

Compounds of the formula the pharmaceutically acceptable salts thereof, wherein Q and R1 are as defined below, and novel carboxylic acid and acid halide intermediates used in the synthesis of such compounds. The compounds of formula I are inhibitors of acyl coenzyme A: cholesterol acyltransferase (ACAT) and are useful as hypolipidemic and antiatherosclerosis agents.