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CAS

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537041-67-1

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.

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  • 537041-67-1 Structure

  • Basic information

    1. Product Name: tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate
    2. Synonyms: tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate
    3. CAS NO:537041-67-1
    4. Molecular Formula: C12H19NO3
    5. Molecular Weight: 225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 537041-67-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate(537041-67-1)
    11. EPA Substance Registry System: tert-butyl 2-(5-methylfuran-2-yl)ethylcarbamate(537041-67-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 537041-67-1(Hazardous Substances Data)

537041-67-1 Usage

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.

537041-67-1SDS

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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