18530-30-8 Usage
Uses
Used in Pharmaceutical Industry:
(+)-CAMPHORCARBOXYLIC ACID is used as an active pharmaceutical ingredient for its antimicrobial properties, making it suitable for the development of drugs targeting various infections.
Used in Fragrance Industry:
(+)-CAMPHORCARBOXYLIC ACID is used as a key component in the formulation of fragrances due to its distinct camphor-like odor, contributing to the overall scent profile of various products.
Used in Medicinal Chemistry:
(+)-CAMPHORCARBOXYLIC ACID is used as a versatile building block in the synthesis of various drugs, leveraging its chemical properties to create new therapeutic agents.
Used in Antimicrobial Applications:
(+)-CAMPHORCARBOXYLIC ACID is used as an antimicrobial agent for its ability to inhibit the growth of microorganisms, making it a valuable compound in the development of antimicrobial products.
Used in Anti-inflammatory and Anti-oxidant Applications:
(+)-CAMPHORCARBOXYLIC ACID is used as an anti-inflammatory and anti-oxidant agent, harnessing its properties to reduce inflammation and oxidative stress in various medical and cosmetic products.
Check Digit Verification of cas no
The CAS Registry Mumber 18530-30-8 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, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18530-30:
(7*1)+(6*8)+(5*5)+(4*3)+(3*0)+(2*3)+(1*0)=98
98 % 10 = 8
So 18530-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c1-10(2)6-4-5-11(10,3)8(12)7(6)9(13)14/h6-7H,4-5H2,1-3H3,(H,13,14)/t6-,7+,11+/m1/s1
18530-30-8Relevant 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.
