508-34-9

Basic information

• Product Name: camphoronic acid
• Synonyms: camphoronic acid;2,3-Dimethyl-1,2,3-butanetricarboxylic acid;[R,(-)]-2,3-Dimethyl-1,2,3-butanetricarboxylic acid
• CAS NO: 508-34-9
• Molecular Formula: C₉H₁₄O₆
• Molecular Weight: 218.2
• Mol File: 508-34-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: camphoronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: camphoronic acid(508-34-9)
• EPA Substance Registry System: camphoronic acid(508-34-9)

Safety Data

• Hazardous Substances Data: 508-34-9(Hazardous Substances Data)

Upstream product

• 858795-21-8 3,4-dicyano-2,2,3-trimethyl-glutaric acid diethyl ester 
• 54812-08-7 4,7,7-trimethyl-2-oxa-bicyclo[2.2.1]heptan-3-one 
• 7697-37-2 nitric acid 
• 7732-18-5 water 
• 465-48-5 4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid 
• 7647-01-0 hydrogenchloride 
• 124-83-4 D-(+)-camphoric acid 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 21733-78-8 1,2,2-trimethyl-3-cyclopentene-1-carboxylic acid 
• 90694-65-8 4-hydroxy-1,2,2-trimethyl-cyclopentanecarboxylic acid 
• 514-12-5 3,3-dibromo-bornan-2-one 
• 464-89-1 camphononic acid 
• 87798-58-1 1,2,2-trimethyl-cyclopent-3-ene-1,3-dicarboxylic acid 
• 448188-10-1 (1R,3S)-1,2,2,3-Tetramethyl-cyclopentanecarboxylic acid 

Relevant articles and documents

Polyethylene Glycols as Efficient Catalysts for the Oxidation of Bicyclic Monoterpenes by Ceric Ammonium Nitrate in Acetonitrile under Acid-Free Conditions: Kinetic and Mechanistic Approach

Polyethylene glycols (PEG) acts as efficient catalysts for the oxidation of bicyclic monoterpenes such as borneol, isoborneol, and camphor by ceric ammonium nitrate (CAN), a laboratory desktop reagent, in acetonitrile medium under mineral acid-free conditions. The kinetics of the reactions revealed first-order dependence on in both [CAN] and [bicyclic terpene]. The rate of oxidation is accelerated with an increase in [PEG] linearly, which could be explained by considering PEG-bound oxidant (PEG-CAN) as more reactive species than (CAN) itself. The mechanism of oxidation in PEG media has been explained through the participation of PEG-bound oxidant (PEG-CAN) and bicyclic monoterpene in the slow step.

TITANIUM TETRACHLORIDE PROMOTED KNOEVENAGEL CONDENSATION OF A STERICALLY HINDERED KETO ESTER. A HIGH YIELD SYNTHESIS OF CAMPHORONIC ACID

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