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537041-67-1

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537041-67-1 Usage

General Description

Tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is a chemical compound that belongs to the carbamate class of compounds. It is a derivative of tert-butyl carbamate and contains a furan ring with a methyl group at the 5-position. tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is commonly used in organic synthesis and medicinal chemistry, and it has shown to have potential pharmacological properties. The tert-butyl group provides steric hindrance and stability to the compound, while the furan ring contributes to its reactivity and biological activity. Overall, tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate is an important chemical with various applications in research and industry.

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.

537041-67-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[2-(5-methylfuran-2-yl)ethyl]carbamate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:537041-67-1 SDS

537041-67-1Downstream Products

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.

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