7063-30-1

Basic information

• Product Name: 6-(5-{[5-cyano-1,4-dimethyl-2-(3-methylpiperidin-1-yl)-6-oxo-1,6-dihydropyridin-3-yl]methylidene}-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)hexanoic acid
• CAS NO: 7063-30-1
• Molecular Formula: C₁₃H₁₇NO
• Molecular Weight: 502.6494
• Mol File: 7063-30-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 553°C at 760 mmHg
• Flash Point: 288.2°C
• Density: 1.37g/cm³
• Vapor Pressure: 1.1E-13mmHg at 25°C
• Refractive Index: 1.656
• CAS DataBase Reference: 6-(5-{[5-cyano-1,4-dimethyl-2-(3-methylpiperidin-1-yl)-6-oxo-1,6-dihydropyridin-3-yl]methylidene}-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)hexanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(5-{[5-cyano-1,4-dimethyl-2-(3-methylpiperidin-1-yl)-6-oxo-1,6-dihydropyridin-3-yl]methylidene}-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)hexanoic acid(7063-30-1)
• EPA Substance Registry System: 6-(5-{[5-cyano-1,4-dimethyl-2-(3-methylpiperidin-1-yl)-6-oxo-1,6-dihydropyridin-3-yl]methylidene}-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)hexanoic acid(7063-30-1)

Safety Data

• Hazardous Substances Data: 7063-30-1(Hazardous Substances Data)

Upstream product

• 6740-84-7 1-Hydroxycyclopentyl-phenylketon-N-methylimin 
• 6740-84-7 1-Hydroxy-cyclopentyl-(phenyl)-N-methylketimin 
• 4631-27-0 2-(methylamino)-2-phenylcyclohexan-1-one hydrochloride 
• 5422-88-8 phenyl cyclopentyl ketone 
• 6740-66-5 (1-bromocyclopentyl)(phenyl)methanone 

Downstream Products

• 64794-75-8 7-aza-11,12-dioxa-7-methyl-6-phenyltricyclo[ 7,2,1,01,6 ]dodecane 
• 4631-27-0 2-(methylamino)-2-phenylcyclohexan-1-one hydrochloride 
• 50-00-0 formaldehyd 
• 7015-50-1 2-amino-2-phenylcyclohexan-1-one 

Relevant articles and documents

ARYLCYCLOHEXYLAMINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF PSYCHIATRIC DISORDERS

Provided herein are arylcyclohexylamine derivatives and their use in the treatment of psychiatric disorders.

Asymmetric catalysis. Part 153: Metal-catalysed enantioselective α-ketol rearrangement

Promoted by catalytic amounts of Ni complexes tertiary α-hydroxyketones 1a, 3a-5a undergo rearrangement, forming chiral isomers 1b, 3b-5b. The best enantioselection was obtained with the model system 1-benzoylcyclopentanol 4a/2-hydroxy-2-phenylcyclohexanone 4b. In a ligand screening 2-[4-(S)-tert-butyloxazolin-2-yl]pyridine gave the highest enantiomeric excess of 46% (S)-4b. The analogous isomerisation reactions of α-hydroxyimines 6a, 7a forming chiral α-aminoketones 6b, 7b were established.