59119-18-5 Usage
General Description
1-Benzyl-4-hydroxy-4-piperidinecarboxylic acid is a chemical compound that belongs to the class of piperidinecarboxylic acids. It is an organic compound with a molecular formula of C16H21NO3 and a molecular weight of 275.34 g/mol. 1-Benzyl-4-hydroxy-4-piperidinecarboxylic acid is a derivative of piperidine and contains a benzyl group and a hydroxy group attached to the piperidine ring. 1-Benzyl-4-hydroxy-4-piperidinecarboxylic acid has potential biological activity and is being studied for its medicinal properties, including its potential use as a pharmaceutical intermediate in the synthesis of various drugs. It is important for researchers and chemists in the pharmaceutical industry due to its potential therapeutic applications and its role as a building block in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 59119-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,1 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59119-18:
(7*5)+(6*9)+(5*1)+(4*1)+(3*9)+(2*1)+(1*8)=135
135 % 10 = 5
So 59119-18-5 is a valid CAS Registry Number.
59119-18-5Relevant articles and documents
Anesthetic compounds and related methods of use
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Page/Page column 67, (2015/11/09)
Provided herein are compounds according to formula (I): Provided herein is also a pharmaceutical composition comprising a compound according to formula (I) and a pharmaceutically acceptable carrier, and a method for providing anesthesia in a subject by administering such a pharmaceutical composition.
Oxazolones as potent inhibitors of 11β-hydroxysteroid dehydrogenase type 1
Sutin, Lori,Andersson, Soeren,Bergquist, Lars,Castro, Victor M.,Danielsson, Eva,James, Stephen,Henriksson, Martin,Johansson, Lars,Kaiser, Christina,Flyren, Katarina,Williams, Meredith
, p. 4837 - 4840 (2008/02/11)
2,5,5-Trisubstituted oxazolones were identified as potent inhibitors of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1). The synthesis, structure-activity relationship and metabolic stability of these compounds are presented.