811842-18-9 Usage
General Description
2-AMINOMETHYL-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER is a chemical compound consisting of a piperidine ring with a benzyl ester attached to the carboxylic acid group. It is commonly used in medicinal chemistry and pharmaceutical research as a building block for the synthesis of various bioactive compounds. This chemical has the potential to exhibit various biological activities, such as acting as a potential drug candidate for the treatment of neurological and psychiatric disorders due to its potential interaction with neurotransmitter receptors. Its structure and functional groups also make it suitable for use as an intermediate in the synthesis of other organic compounds. Furthermore, it is important to handle, store, and use this chemical in a controlled manner due to its potential health hazards and environmental impact if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 811842-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,8,4 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 811842-18:
(8*8)+(7*1)+(6*1)+(5*8)+(4*4)+(3*2)+(2*1)+(1*8)=149
149 % 10 = 9
So 811842-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O2/c15-10-13-8-4-5-9-16(13)14(17)18-11-12-6-2-1-3-7-12/h1-3,6-7,13H,4-5,8-11,15H2
811842-18-9Relevant articles and documents
Active agent prodrugs with heterocyclic linkers
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Page/Page column 143; 144; 145, (2015/10/28)
The embodiments provide prodrug compounds of Formulae I-XVII. The present disclosure also provides compositions, and their methods of use, where the compositions comprise a prodrug compound of Formulae I-XVII that provides controlled release of an active agent. Such compositions can optionally provide a trypsin inhibitor that interacts with the enzyme that mediates the controlled release of an active agent from the prodrug so as to attenuate enzymatic cleavage of the prodrug.