56098-50-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(chloromethyl)piperidine hydrochloride is used as a key intermediate in the synthesis of various pharmaceutical drugs for its ability to modulate neurotransmitters and contribute to the development of pharmacological agents.
Used in Organic Chemistry:
2-(chloromethyl)piperidine hydrochloride is used as a building block in the synthesis of organic compounds, leveraging its unique chemical properties to create a wide range of products.
Used in Pesticide Production:
2-(chloromethyl)piperidine hydrochloride is used as a precursor in the production of pesticides, contributing to the development of effective and targeted pest control agents.
Used in Drug Discovery:
2-(chloromethyl)piperidine hydrochloride is utilized in drug discovery processes for its potential to form the basis of new and innovative pharmaceutical compounds, enhancing the search for novel treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 56098-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,9 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56098-50:
(7*5)+(6*6)+(5*0)+(4*9)+(3*8)+(2*5)+(1*0)=141
141 % 10 = 1
So 56098-50-1 is a valid CAS Registry Number.
56098-50-1Relevant academic research and scientific papers
Evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase
Shankaran,Donnelly, Karla L.,Shah, Shrenik K.,Guthikonda, Ravindra N.,MacCoss, Malcolm,Humes, John L.,Pacholok, Stephen G.,Grant, Stephan K.,Kelly,Wong
, p. 4539 - 4544 (2007/10/03)
Syntheses and evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2- imines as inhibitors of nitric oxide synthase (NOS) are discussed. An extensive SAR was established for pyrrolidin-2-imines class of compounds. The amidines came out as the most potent inhibitors in addition to displaying selectivity.
Synthesis of substituted piperidines, indolizidines, quinolizidines, and pyrrolizidines via a cycloaddition strategy using acetylenic sulfones as alkene dipole equivalents
Back, Thomas G.,Nakajima, Katsumasa
, p. 261 - 263 (2008/02/13)
(equation presented) The conjugate additions of β- and γ-chloroamines to acetylenic sulfones afford enamine sulfones, which then undergo intramolecular alkylation to produce the corresponding cyclic enamines. This provides a convenient route to substitute
