474-98-6 Usage
Uses
Used in Pharmaceutical Industry:
(+/-)-Camphorcarboxylic acid is used as a starting material for the synthesis of various pharmaceuticals due to its versatile chemical properties and potential therapeutic effects.
Used in Anti-inflammatory and Analgesic Applications:
(+/-)-Camphorcarboxylic acid is used as an anti-inflammatory and analgesic agent, providing relief from pain and reducing inflammation in various conditions.
Used in Anti-tumor Applications:
(+/-)-Camphorcarboxylic acid is used as a potential anti-tumor agent, with ongoing research exploring its effects on inhibiting tumor growth and progression.
Used in Anti-microbial Applications:
(+/-)-Camphorcarboxylic acid is used as a potential anti-microbial agent, with studies investigating its ability to combat various microbial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 474-98-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 474-98:
(5*4)+(4*7)+(3*4)+(2*9)+(1*8)=86
86 % 10 = 6
So 474-98-6 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
474-98-6Relevant 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.
