560-05-4 Usage
Uses
Used in Pharmaceutical Industry:
DL-Camphoric acid is used as a starting material for the production of pharmaceuticals due to its ability to serve as a chiral resolving agent, which is essential in the synthesis of various medicinal compounds.
Used in Fragrance Industry:
It is utilized as a starting material for the production of fragrances, capitalizing on its unique properties to create a wide array of scent profiles.
Used in Flavoring Industry:
DL-Camphoric acid is employed in the creation of flavoring agents, leveraging its chemical structure to impart specific tastes in food and beverage products.
Used in Synthesis of Camphor Derivatives:
It serves as a precursor in the synthesis of camphor derivatives, which have a variety of industrial and medicinal applications, further expanding its utility in chemical processes.
Used in Organic Chemistry Research:
DL-Camphoric acid is used in research for its potential anti-inflammatory and antimicrobial properties, indicating its potential as a compound of interest for developing new therapeutic agents and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 560-05-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 560-05:
(5*5)+(4*6)+(3*0)+(2*0)+(1*5)=54
54 % 10 = 4
So 560-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)
560-05-4Relevant academic research and scientific papers
Oxidative cleavage of α-diketones using tetraethylammonium bromide as phase transfer catalyst
Singh, Sundaram,Singh, Manorama,Singh, Krishna Nand
, p. 88 - 90 (2007/10/03)
The efficient use of tetraethylammonium bromide as phase transfer catalyst has led to explore synthetically useful reactions of tetraethylammonium superoxide with a variety of α-diketones.The substrates, furil 1a, 4,4'-dimethylbenzil 1b, 4,4'-dimethoxybenzil 1c, 4,4'-dibromobenzil 1d, 9,10-phenanthroquinone 1e, 1,2-naphthoquinone 1f, (+/-) camphorquinone 1g and 2,2'-pyridil 1h are oxidatively cleaved to furnish 2-furancarboxylic acid 2a, p-methylbenzoic acid 2b, p-methoxybenzoic acid 2c, p-bromobenzoic acid 2d, 2,2'-biphenylcarboxylic acid 2e, phthalic acid 2f, (+/-)-camphoric acid 2g and 2-pyridinecarboxylic acid 2h respectively, in reasonably good yields under the present set of mild reaction conditions.
