18530-29-5 Usage
Uses
Used in Organic Synthesis:
(-)-Camphorcarboxylic acid is used as a chiral building block in organic synthesis for the creation of enantiomerically pure compounds. Its unique stereochemistry allows for the development of complex molecules with specific biological activities.
Used in Pharmaceutical Industry:
(-)-Camphorcarboxylic acid is used as a precursor for the synthesis of pharmaceuticals. Its versatile structure makes it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
(-)-Camphorcarboxylic acid is also used as a precursor in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Traditional Medicine:
(-)-Camphorcarboxylic acid has been used in traditional medicine for its potential anti-inflammatory and analgesic effects, providing relief from pain and reducing inflammation in various conditions.
Used in Aromatherapy:
Due to its distinct odor, (-)-camphorcarboxylic acid has been utilized in aromatherapy for its potential mood-enhancing and relaxing properties, contributing to overall well-being and stress reduction.
Check Digit Verification of cas no
The CAS Registry Mumber 18530-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,3 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18530-29:
(7*1)+(6*8)+(5*5)+(4*3)+(3*0)+(2*2)+(1*9)=105
105 % 10 = 5
So 18530-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-5-7(4)8(9)6(2)3/h6-7H,5H2,1-4H3
18530-29-5Relevant academic research and scientific papers
Synthesis and local anesthetic activity of some derivatives of N,N-diethyl-2-(2-alkoxyphenylcarbamoyloxy)bornan-3-ylmethyl-ammonium chlorides
Gregan,Kettmann,Novomesky,Racanska,Svec
, p. 375 - 385 (2007/10/02)
A series of 8 new esters of 2-alkoxyphenyl-carbamoic acid were synthesized and assayed for local anesthetic activity. All compounds were isolated as hydrochlorides and their structure was proved by 1H-NMR 13C-NMR and IR spectroscopy. The index of anesthetic activity in infiltration and surface anesthesia proved that all prepared compounds are significantly more active than the standard reference compounds, procaine and cocaine, respectively; it is tightly correlated with the length of the alkoxy group. It was found that there is a parabolic relationship between log activity and molecular lipophilicity (as measured by R(M)). Toxicity of all compounds is within acceptable limits.
