182808-28-2 Usage
Description
ETHYL 4-CYANOPIPERIDINE-1-CARBOXYLATE, with the CAS number 182808-28-2, is a compound that is utilized in the field of organic synthesis. It is characterized by its colorless oil appearance, which is a common property for many organic compounds.
Uses
Used in Organic Synthesis:
ETHYL 4-CYANOPIPERIDINE-1-CARBOXYLATE is used as a synthetic intermediate for the creation of various chemical compounds. Its unique structure allows it to be a valuable building block in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
As an organic synthesis intermediate, ETHYL 4-CYANOPIPERIDINE-1-CARBOXYLATE is particularly useful due to its reactivity and functional groups, which can be further modified or incorporated into more complex molecules. This makes it a versatile compound in the development of new and innovative products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 182808-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,8,0 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 182808-28:
(8*1)+(7*8)+(6*2)+(5*8)+(4*0)+(3*8)+(2*2)+(1*8)=152
152 % 10 = 2
So 182808-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O2/c1-2-13-9(12)11-5-3-8(7-10)4-6-11/h8H,2-6H2,1H3
182808-28-2Relevant articles and documents
Nickel-Catalyzed Cyanation of Unactivated Alkyl Sulfonates with Zn(CN)2
Xia, Aiyou,Lv, Peizhuo,Xie, Xin,Liu, Yuanhong
, p. 7842 - 7847 (2020/11/02)
Cyanation of unactivated primary and secondary alkyl mesylates with Zn(CN)2 catalyzed by nickel has been developed. The reaction provides an efficient route for the synthesis of alkyl nitriles with wide substrate scope, good functional group tolerance, and compatibility with heterocyclic compounds. Mechanistic studies indicate that alkyl iodide generated in situ serves as the reactive intermediate and the gradual release of alkyl iodide is crucial for the success of the reaction.
Preparation of spiro[cyclopent[b]indole-3,4'-piperidine] derivatives as acetylcholinesterase and monoamine oxidase inhibitors.
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, (2008/06/13)
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