43032-38-8 Usage
Uses
Used in Pharmaceutical Industry:
3-(PIPERAZIN-1-YL)PROPIONIC ACID ETHYL ESTER is used as a precursor in the synthesis of various drugs for its ability to contribute to the development of medications with significant therapeutic effects. It is particularly instrumental in the creation of antipsychotic and antidepressant medications, where its chemical properties facilitate the production of these critical compounds.
Used in Prostaglandin and Leukotriene Synthesis:
3-(PIPERAZIN-1-YL)PROPIONIC ACID ETHYL ESTER is used as a precursor to prostaglandin and leukotriene endoperoxides, playing a crucial role in the biological processes involving these compounds. Its involvement in the synthesis of these endoperoxides highlights its importance in the broader scope of pharmaceutical and medical research.
Used as a Chemical Intermediate:
In the production of other pharmaceuticals and research chemicals, 3-(PIPERAZIN-1-YL)PROPIONIC ACID ETHYL ESTER serves as a valuable chemical intermediate. Its versatility in chemical reactions and synthesis processes makes it an essential component in the development of a range of pharmaceutical products, contributing to the advancement of medical treatments and scientific understanding.
Check Digit Verification of cas no
The CAS Registry Mumber 43032-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 43032-38:
(7*4)+(6*3)+(5*0)+(4*3)+(3*2)+(2*3)+(1*8)=78
78 % 10 = 8
So 43032-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O2/c1-2-13-9(12)3-6-11-7-4-10-5-8-11/h10H,2-8H2,1H3
43032-38-8Relevant academic research and scientific papers
COMPOSITIONS OF NOVEL OPIOID COMPOUNDS AND METHOD OF USE THEREOF
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Page/Page column 65, (2010/11/24)
Diarylmethylpiperazine compounds are described, which are useful as mu and/or delta receptor opioid compounds, without central side effects. Pharmaceutical compositions containing such compounds are variously useful for peripheral or non-centrally mediated indications, including peripherally mediated and neuropathic pain, urogenital tract disorders, overactive bladder, urinary incontinence, sexual disorders, premature ejaculation, cough, lung edema, cardiac disorders, cardioprotection, gastro-intestinal disorders, diarrhea, irritable bowl syndrome, functional distention, immuno-modulation and anti-tumor activity.
Spirocyclic nonpeptide glycoprotein IIb-IIIa antagonists. Part 3: Synthesis and SAR of potent and specific 2,8-diazaspiro[4.5]decanes
Mehrotra, Mukund M.,Heath, Julie A.,Rose, Jack W.,Smyth, Mark S.,Seroogy, Joseph,Volkots, Deborah L.,Ruhter, Gerd,Schotten, Theo,Alaimo, Lisa,Park, Gary,Pandey, Anjali,Scarborough, Robert M.
, p. 1103 - 1107 (2007/10/03)
The synthesis and biological activity of analogues containing spiro piperidinylpyridine and pyrrolidinylpyridine templates are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of the spiro structures as central template for nonpeptide RGD mimics.
