75621-22-6

Basic information

• Product Name: cyclohexane-2,2,6,6-d4-carboxylic acid
• Synonyms: cyclohexane-2,2,6,6-d4-carboxylic acid
• CAS NO: 75621-22-6
• Molecular Weight: 132.139
• Mol File: 75621-22-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: cyclohexane-2,2,6,6-d4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohexane-2,2,6,6-d4-carboxylic acid(75621-22-6)
• EPA Substance Registry System: cyclohexane-2,2,6,6-d4-carboxylic acid(75621-22-6)

Safety Data

• Hazardous Substances Data: 75621-22-6(Hazardous Substances Data)

Upstream product

• 3452-02-6 2,2,6,6-tetradeuterio-1-methylenecyclohexane 
• 1006-03-7 cyclohexanone-2,2,6,6-d4 
• 75621-20-4 cyclohexyl-2,2,6,6-d4-methanol 
• 114954-78-8 1-hydroxy<2,2,6,6-(2)H4>cyclohexanecarboxylic acid 
• 108-94-1 cyclohexanone 

Downstream Products

• 75621-24-8 methyl 1-methylcyclohexane-2,2,6,6-d4-carboxylate 
• 75621-25-9 (1-methylcyclohexyl-2,2,6,6-d4)methanol 
• 75621-23-7 methyl cyclohexane-2,2,6,6-d4-carboxylate 

Relevant articles and documents

Lactone Formation in Superacidic Media

The reaction of substituted 1-hydroxycyclohexanecarboxylic acids in fluorosulphuric acid has been studied.Cyclisation takes place around 0 deg C, accompanied by rearrangement in appropriate cases, yielding the thermodynamically stable lactone or mixture of lactones.An unexpected feature of these reactions is that the carboxy-substituted cyclohexyl carbocation does not undergo ring contraction, unlike the unsubstituted cyclohexyl carbocation, although the cycloheptyl system contracts to cyclohexyl.We suggest that the cyclohexyl carbocation is strongly stabilised by carboxyl substitution, as a result of through-space interaction between the carboxyl oxygen atom and the carbocation centre.