130275-56-8 Usage
Description
Methyl 3-(2,6-dimethylpiperidin-1-yl)propanoate is a chemical compound with the molecular formula C12H23NO2. It is a methyl ester derivative of a piperidine-derived compound, often used as an intermediate in organic synthesis and pharmaceutical development. methyl 3-(2,6-dimethylpiperidin-1-yl)propanoate has a pungent odor and is soluble in organic solvents such as ethanol and ethyl acetate.
Uses
Used in Pharmaceutical Industry:
Methyl 3-(2,6-dimethylpiperidin-1-yl)propanoate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new medications.
Used in Agrochemical Industry:
methyl 3-(2,6-dimethylpiperidin-1-yl)propanoate serves as an intermediate in the production of agrochemicals, where it can be used to create substances that help protect crops and enhance agricultural productivity.
Used in Fine Chemicals Production:
Methyl 3-(2,6-dimethylpiperidin-1-yl)propanoate is used as a building block in the synthesis of other fine chemicals, which are high-purity, high-value chemicals used in various specialized applications.
Used in Fragrance and Flavoring Industry:
It is also utilized in the production of fragrances and flavorings, where its unique chemical structure can contribute to the creation of distinct scents and tastes in consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 130275-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,7 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130275-56:
(8*1)+(7*3)+(6*0)+(5*2)+(4*7)+(3*5)+(2*5)+(1*6)=98
98 % 10 = 8
So 130275-56-8 is a valid CAS Registry Number.
130275-56-8Relevant articles and documents
Synthesis and Antiarrhythmic Activity of cis-2,6-Dimethyl-α,α-diaryl-1-piperidinebutanols
Hoefle, M. L.,Blouin, L. T.,Fleming, R. W.,Hastings, S.,Hinkley, J. M.,et al.
, p. 12 - 19 (2007/10/02)
A series of α,α-diaryl-1-piperidinebutanols was evaluated for antiarrhythmic activity in the coronary ligated dog model.Structure-activity relationship studies indicated that the 2,6-dimethylpiperidine group yielded compounds with the best antiarrhythmic
