878130-38-2 Usage
Description
Tert-butyl 4-(cyanomethyl)-4-(4-methoxyphenyl)piperidine-1-carboxylate is a complex chemical compound featuring a piperidine ring with a tert-butyl group and a cyanomethyl group attached to it, as well as a 4-methoxyphenyl group. tert-butyl 4-(cyanomethyl)-4-(4-methoxyphenyl)piperidine-1-carboxylate may have potential pharmaceutical applications due to the known properties of piperidine derivatives, which have been studied for their antiviral, antipsychotic, and analgesic properties. The presence of the cyanomethyl group also suggests that this compound could be a valuable building block in organic synthesis, particularly for the development of new drugs or materials. Further research is necessary to fully understand its properties and potential uses.
Uses
Used in Pharmaceutical Industry:
Tert-butyl 4-(cyanomethyl)-4-(4-methoxyphenyl)piperidine-1-carboxylate is used as a potential pharmaceutical candidate for [application reason] due to its structural features and the known properties of related piperidine derivatives, which have demonstrated antiviral, antipsychotic, and analgesic effects.
Used in Organic Synthesis:
In the field of organic synthesis, tert-butyl 4-(cyanomethyl)-4-(4-methoxyphenyl)piperidine-1-carboxylate is used as a building block for the development of new drugs or materials, leveraging the cyanomethyl group for further chemical reactions and innovations in drug design.
Check Digit Verification of cas no
The CAS Registry Mumber 878130-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,1,3 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 878130-38:
(8*8)+(7*7)+(6*8)+(5*1)+(4*3)+(3*0)+(2*3)+(1*8)=192
192 % 10 = 2
So 878130-38-2 is a valid CAS Registry Number.
878130-38-2Relevant articles and documents
Synthesis of 4-substituted piperidines via a mild and scalable two-step Cu2O-mediated decarboxylation of cyanoesters
Chauder, Brian A.,Boros, Eric E.,Du, Kien S.,Kazmierski, Wieslaw M.,Koble, Cecilia S.,Thompson, James B.,Tabet, Elie A.
, p. 279 - 284 (2007/10/03)
A four-step, high-yielding, kilogram-scale protocol to prepare aldehyde 5 is reported. The key reaction is a mild, two-step Cu2O-mediated decarboxylation of cyanoester 3 that proceeds in excellent yield. The general applicability of this method
