144220-38-2 Usage
Description
Benzenesulfenamide, N-(5-phenyl-4-pentenyl)-N-2-propenyl-, (E)-, also known as N-allyl-N-(5-phenyl-4-pentenyl)benzenesulfonamide, is a chemical compound with the molecular formula C18H21NS. It belongs to the sulfenamide class of organic compounds, characterized by a sulfur-nitrogen double bond (S=N) and a sulfonamide functional group (-SO2NH2). This unique structure endows it with potential applications in the production of pharmaceuticals and agrochemicals, as well as in organic synthesis and medicinal chemistry research.
Uses
Used in Pharmaceutical Industry:
Benzenesulfenamide, N-(5-phenyl-4-pentenyl)-N-2-propenyl-, (E)is used as an intermediate in the synthesis of pharmaceuticals for its unique sulfur-nitrogen double bond and sulfonamide functional group. These features allow for the development of new drug candidates with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Benzenesulfenamide, N-(5-phenyl-4-pentenyl)-N-2-propenyl-, (E)is utilized as a precursor in the production of agrochemicals. Its chemical structure can be modified to create compounds with pesticidal or herbicidal properties, contributing to the development of more effective and environmentally friendly agricultural products.
Used in Organic Synthesis:
Benzenesulfenamide, N-(5-phenyl-4-pentenyl)-N-2-propenyl-, (E)serves as a valuable building block in organic synthesis. Its sulfur-nitrogen double bond and sulfonamide group can be employed in various chemical reactions, enabling the synthesis of a wide range of organic compounds with diverse applications.
Used in Medicinal Chemistry Research:
As a chemical compound with a unique structure, Benzenesulfenamide, N-(5-phenyl-4-pentenyl)-N-2-propenyl-, (E)is an interesting candidate for further research in medicinal chemistry. Its properties can be explored to understand its potential interactions with biological targets, leading to the discovery of new therapeutic agents and insights into drug design.
Check Digit Verification of cas no
The CAS Registry Mumber 144220-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144220-38:
(8*1)+(7*4)+(6*4)+(5*2)+(4*2)+(3*0)+(2*3)+(1*8)=92
92 % 10 = 2
So 144220-38-2 is a valid CAS Registry Number.
144220-38-2Relevant articles and documents
Synthesis of pyrrolizidines using aminyl radicals generated from sulfenamide precursors
Russell Bowman,Clark, David N.,Marmon, Robert J.
, p. 1295 - 1310 (2007/10/02)
Tandem radical cyclisations of aminyl radicals generated from sulfenamide precursors have been used for the synthesis of pyrrolizidines and other polycyclic nitrogen heterocycles. The aminyl radicals are generated by reaction between sulfenamide precursor
