101347-72-2 Usage
Uses
Used in Organic Synthesis:
Pyrrolidine, 1-acetyl-4-ethyl-2-methyl-, trans(9CI) is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure and trans-configuration facilitate specific reactions that are essential for the development of new compounds.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, Pyrrolidine, 1-acetyl-4-ethyl-2-methyl-, trans(9CI) serves as a crucial component in the synthesis of drugs. Its properties allow for the production of medicinal compounds with desired therapeutic effects.
Used in Agrochemical Production:
Pyrrolidine, 1-acetyl-4-ethyl-2-methyl-, trans(9CI) is also employed in the development of agrochemicals, contributing to the creation of products that enhance crop protection and agricultural yield.
Used in Specialty Chemicals:
Pyrrolidine, 1-acetyl-4-ethyl-2-methyl-, trans(9CI) finds application in the production of specialty chemicals, where its distinctive attributes are leveraged to achieve specific outcomes in various industrial applications.
It is important to handle Pyrrolidine, 1-acetyl-4-ethyl-2-methyl-, trans(9CI) with care, adhering to proper safety guidelines and regulations to ensure safe and effective use in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 101347-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,4 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101347-72:
(8*1)+(7*0)+(6*1)+(5*3)+(4*4)+(3*7)+(2*7)+(1*2)=82
82 % 10 = 2
So 101347-72-2 is a valid CAS Registry Number.
101347-72-2Relevant academic research and scientific papers
PYRROLIDINES BY INTRAMOLECULAR ADDITION OF KOLBE RADICALS GENERATED FROM β-ALLYLAMINOALKANOATES
Becking, L.,Schaefer, H. J.
, p. 2797 - 2800 (2007/10/02)
3-Alkyl-substituted pyrrolidines 7 are obtained by Kolbe electrolysis of β-llylaminoalkanoates 5, intramolecular addition of the radical nd mixed coupling with the radical of a coacid.
