54151-70-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Piperidin-1-yl-propylamine is used as an intermediate in the synthesis of selective serotonin receptor inhibitors for its role in creating compounds that can modulate serotonin levels, which is vital for treating various neurological and psychiatric disorders.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Piperidin-1-yl-propylamine is employed as an intermediate for the development of agrochemicals, contributing to the creation of products that enhance crop protection and yield.
Used in Specialty Chemicals Production:
2-Piperidin-1-yl-propylamine is used as a precursor in the synthesis of specialty chemicals, where its unique properties allow for the development of compounds with specific applications in various industries.
Used in Rubber Industry:
2-Piperidin-1-yl-propylamine is utilized in the production of rubber antioxidants and vulcanizing agents, playing a critical role in enhancing the durability and performance of rubber products.
Used in Organic Compounds Synthesis:
As a reagent, 2-Piperidin-1-yl-propylamine is used in the synthesis of various organic compounds, showcasing its broad applicability in organic chemistry and the creation of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 54151-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,5 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54151-70:
(7*5)+(6*4)+(5*1)+(4*5)+(3*1)+(2*7)+(1*0)=101
101 % 10 = 1
So 54151-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2/c1-8(7-9)10-5-3-2-4-6-10/h8H,2-7,9H2,1H3
54151-70-1Relevant academic research and scientific papers
DIRECT NUCLEOPHILIC SUBSTITUTION IN 2-HALOALKYLAMINES: NEW ROUTE TO SUBSTITUTED ETHYLENEDIAMINES
Chechik, V. O.,Bobylev, V. A.
, p. 1501 - 1502 (2007/10/03)
Nucleophilic substitution in 2-haloalkylamines in weakly polar media was found to proceed partially without intermediate formation of aziridines.This makes it possible to obtain pure substituted ethylenediamines.
