537041-67-1 Usage
Description
Tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is a carbamate class chemical compound that is a derivative of tert-butyl carbamate. It features a furan ring with a methyl group at the 5-position, which contributes to its reactivity and biological activity. The tert-butyl group provides steric hindrance and stability to the compound. This important chemical is utilized in various applications in research and industry.
Uses
Used in Organic Synthesis:
Tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is used as an intermediate in organic synthesis for its reactivity and stability, allowing for the creation of a variety of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is used as a building block for the development of potential pharmaceuticals, leveraging its pharmacological properties and structural features to design new drugs.
Used in Research:
Tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is utilized in research settings to study the effects of structural modifications on the biological activity of compounds, contributing to the advancement of chemical and pharmaceutical sciences.
Used in Industry:
tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is also used in the industry for the production of specialty chemicals and materials, taking advantage of its unique properties to create innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 537041-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,0,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 537041-67:
(8*5)+(7*3)+(6*7)+(5*0)+(4*4)+(3*1)+(2*6)+(1*7)=141
141 % 10 = 1
So 537041-67-1 is a valid CAS Registry Number.
537041-67-1Relevant articles and documents
Preparation of tricyclic nitrogen heterocycle via Intramolecular Diels-Alder reaction
Demircan, Aydin,Parsons, Philip J.
, p. 531 - 536 (2007/10/03)
Preparation of rigid tricyclic nitrogen heterocycles under radicalic condition has been studied. Cyclisation is performed by Diels-Alder ring closure after radicalic hydrogenation. We did not observe any radicalic Cycloaddition / Fragmentation product 12. Tri-n-butyltin hydride (TBTH) and azobisisobutyronitrile were used in toluene or benzene to generate radicalic condition. Intramolecular Diels-Alder (IMDA) reaction on substituted furan species gave tricyclic heterocycle.
