122518-92-7

Basic information

• Product Name: 1,2-Cyclohexanedimethanol, 1,6-dimethyl-, (1R,2S,6S)-
• CAS NO: 122518-92-7
• Molecular Formula: C10H20O2
• Molecular Weight: 172.268
• Mol File: 122518-92-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2-Cyclohexanedimethanol, 1,6-dimethyl-, (1R,2S,6S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclohexanedimethanol, 1,6-dimethyl-, (1R,2S,6S)-(122518-92-7)
• EPA Substance Registry System: 1,2-Cyclohexanedimethanol, 1,6-dimethyl-, (1R,2S,6S)-(122518-92-7)

Safety Data

• Hazardous Substances Data: 122518-92-7(Hazardous Substances Data)

Upstream product

• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 98540-10-4 Acetic acid (1S,2R,6R)-8-chloro-1,2-dimethyl-bicyclo[4.2.0]oct-7-en-7-yl ester 
• 488856-90-2 2-chloro-2,3-dimethyl-cyclohexanone 
• 98540-05-7 dichlorocyclobutanone 
• 1502-24-5 2,3-dimethylcyclohexan-1-ol 
• 1759-64-4 1,6-dimethyl-1-cyclohexene 
• 2409-87-2 methyl (2E)-penta-2,4-dienoate 
• 147219-88-3 {[(2E)-penta-2,4-diene-1-yloxy]methyl}benzene 
• 21651-12-7 (E)-2,4-pentadienoic acid 
• 4949-20-6 (E)-2,4-pentadien-1-ol 
• 98540-06-8 (1R,2S,6S)-1,6-dimethylcyclohexane-1,2-dicarboxylic acid 
• 325981-97-3 (3R,3aS,7S,7aR)-3-Benzyloxymethyl-7,7a-dimethyl-hexahydro-isobenzofuran-1-one 
• 325981-92-8 (3R,3aS,7S,7aR)-3-Benzyloxymethyl-7-methyl-hexahydro-isobenzofuran-1-one 
• 325982-00-1 (R)-1-((1S,2R,3S)-2-Hydroxymethyl-2,3-dimethyl-cyclohexyl)-ethane-1,2-diol 

Downstream Products

• 19906-72-0 bakkenolide A 
• 19906-72-0 (+/-)-bakkenolide A 
• 19906-72-0 (+/-)-7-epi-bakkenolide A 
• 98540-12-6 (+/-)-(1R,2S,6S)-1,2-bis(iodomethyl)-1,6-dimethylcyclohexane 
• 122518-93-8 (1R,2S,6S)-1,2-bis-iodomethyl-1,6-dimethylcyclohexane 

Relevant articles and documents

Core structure of eremophilanes and bakkanes through niobium catalyzed Diels-Alder reaction: Synthesis of (±)-bakkenolide A

A suitable intermediate for the synthesis of eremophilanes and bakkanes was prepared by a highly regioselective and stereoselective one-step synthesis through a niobium catalyzed Diels-Alder reaction. As a demonstration of the versatility of this intermed

Regiocontrol of radical cyclization by Lewis acids. Efficient synthesis of optically active functionalized cyclopentanes and cyclohexanes

(equation presented) Treatment of α-alkylidenelactones 3a-d with Bu3SnH and a catalytic amount of Et3B effected a 5-exo radical cyclization preferentially to provide the corresponding 1 and 2 in a ratio of 70:30 to 100:0. Meanwhile,

An Approach to the Bakkanes. A Short, Stereocontrolled Total Synthesis of (+/-)-Bakkenolide A

A stereoselective total synthesis of (+/-)-bakkenolide A (fukinanolide) has been efficiently achieved in six steps.