164926-88-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Piperidineacetonitrile,1-methylis used as a key intermediate in the synthesis of various pharmaceutical compounds for its high reactivity and versatility in organic synthesis. It contributes to the development of new drugs and medicines by facilitating the creation of complex molecular structures.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Piperidineacetonitrile,1-methylserves as a crucial building block in the production of pesticides and other agrochemicals. Its reactivity allows for the synthesis of effective compounds designed to protect crops and enhance agricultural productivity.
Used in Chemical Processes:
Beyond its applications in pharmaceuticals and agrochemicals, 4-Piperidineacetonitrile,1-methylis utilized in various other chemical processes. Its role as an intermediate aids in the production of a wide range of organic compounds for different industrial applications, showcasing its broad utility in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 164926-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,9,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 164926-88:
(8*1)+(7*6)+(6*4)+(5*9)+(4*2)+(3*6)+(2*8)+(1*8)=169
169 % 10 = 9
So 164926-88-9 is a valid CAS Registry Number.
164926-88-9Relevant articles and documents
INDOL-2-ONE DERIVATIVES DISUBSTITUTED IN THE 3-POSITION, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
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Page/Page column 11, (2010/08/22)
The present invention relates to 3-disubstituted indol-2-one derivatives, to their preparation and to their therapeutic application.
Conformationally restricted thiazole derivatives as novel class of 5-HT3 receptor ligands
Perrone,Berardi,Colabufo,Tortorella,Lograno,Daniele,Govoni
, p. 77 - 82 (2007/10/02)
A new series of tricyclic derivatives of 2-methyl-naphtho[1,2-d] thiazole were synthesized in order to investigate the effects of the conformational restriction of bicyclic thiazole derivatives previously reported on the 5-HT3 receptor affinity. The basic moiety in these compounds is represented by the terminal nitrogen of N-methyl-piperazine or N-methyl-piperidine ring-linked at 2-methyl. All the tricyclic derivatives have a significant 5-HT3 receptor binding affinity and the terminal piperazine ring is more suitable than piperidine one.
