152212-38-9

Basic information

• Product Name: Cyclohexanecarboxylic acid, 1-methyl-2-oxo-, (+)- (9CI)
• Synonyms: (+)-1-methyl-2-oxocyclohexanecarboxylicacid
• CAS NO: 152212-38-9
• Molecular Formula: C8H12O3
• Molecular Weight: 156.18
• Product Categories: CARBOXYLICACID
• Mol File: 152212-38-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclohexanecarboxylic acid, 1-methyl-2-oxo-, (+)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxylic acid, 1-methyl-2-oxo-, (+)- (9CI)(152212-38-9)
• EPA Substance Registry System: Cyclohexanecarboxylic acid, 1-methyl-2-oxo-, (+)- (9CI)(152212-38-9)

Safety Data

• Hazardous Substances Data: 152212-38-9(Hazardous Substances Data)

Upstream product

• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 66088-37-7 ethyl 1-methyl-2-oxocyclohexancarboxylate 
• 124-38-9 carbon dioxide 
• 32116-69-1 2-n-Butylthiomethylen-cyclohexanon 

Downstream Products

• 666260-23-7 racemate trans-2-hydroxy-1-methylcyclohexanecarboxylic acid 
• 666260-23-7 (+)-(1S,2R)-2-hydroxy-1-methylcyclohexane carboxylic acid 
• 812639-07-9 (2S)-2-methyl-2-(2-propen-1-yl)cyclohexanone 

Relevant articles and documents

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Rhodium generated carbonyl ylides with p-quinones: Synthesis of oxa-bridged polycyclic systems

A series of α-diazo carbonyl compounds tethered to substituted cyclopentanone and cyclohexanone units with different tether lengths have been synthesized using diazomethane solution or methanesulphonyl azide. The above synthesized α-diazo carbonyl compounds with rhodium(II) acetate dimer furnish cyclic five- or six-membered-ring carbonyl ylide dipoles, which undergo facile 1,3-dipolar cycloaddition with p-quinones to furnish various novel oxa-bridged polycyclic systems 10, 13 and 11, 14 as C=C and C=O addition products of p-quinones. Very interesting unusual cyclization product, tri-oxapolycyclic compounds 12 and 15 were also obtained. Single-crystal X-ray analyses of 11a, 12d and 14a are reported to firmly establish the structure and stereochemistry of the oxa-bridged polycyclic systems. The molecules 11a and 14a exhibit novel C-H···O hydrogen bonding motif in the crystal structure. On the other hand, the molecule 12d revealed both O-H···O and C-H···O motifs in the solid-state architecture.