24252-38-8 Usage
General Description
1-Ethylpiperidine-4-carboxylic acid ethyl ester is a chemical compound with the formula C12H21NO2. It is an ester of 1-ethylpiperidine-4-carboxylic acid, which is a derivative of piperidine. 1-ETHYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER has potential applications in pharmaceutical research and development as a building block for the synthesis of various bioactive compounds. It is also used as a precursor in the production of other chemicals and pharmaceutical ingredients. The compound is a colorless to pale yellow liquid with a characteristic piperidine odor and is typically handled and stored under controlled conditions due to its reactivity and potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 24252-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24252-38:
(7*2)+(6*4)+(5*2)+(4*5)+(3*2)+(2*3)+(1*8)=88
88 % 10 = 8
So 24252-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H19NO2/c1-3-11-7-5-9(6-8-11)10(12)13-4-2/h9H,3-8H2,1-2H3
24252-38-8Relevant articles and documents
SUBSTITUTED BENZAZOLES AND USE THEREOF AS INHIBITORS OF RAF KINASE
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Page/Page column 40, (2008/06/13)
New substituted benzazole compounds of formula (I), compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additi
Synthesis and pharmacological evaluation of a new class of 2-oxo-8- azaspiro (4,5)decan-1-ones as analogues of the muscarinic agonist RS-86
Cignarella,Villa,Barlocco
, p. 1439 - 1445 (2007/10/02)
A new series of 8-substituted-2-oxo-8-azapsiro (4,5)decan-1-ones has been synthesized and compounds tested for their cholinergic properties in comparison with the muscarinic agonist RS-86. Preliminary in vitro and in vivo pharmacological data indicate that none of them is provided with significant cholinergic effects either at central or peripheral level. A possible explanation for the lack of activity is given on the basis of conformational studies.
