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Ethyl N-(3-ethoxycarbonylaminophenyl)carbamate is a chemical compound with the molecular formula C11H14N2O4. It is an ester derivative of carbamic acid, featuring an ethyl group attached to the nitrogen atom of the carbamate functional group. The compound has a phenyl ring with an ethoxycarbonylamino substituent at the 3-position, which contributes to its chemical reactivity and properties. This organic compound is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for further functionalization and modification, making it a versatile building block in organic chemistry.

7450-61-5

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7450-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7450-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7450-61:
(6*7)+(5*4)+(4*5)+(3*0)+(2*6)+(1*1)=95
95 % 10 = 5
So 7450-61-5 is a valid CAS Registry Number.

7450-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(3-ethoxycarbonylaminophenyl)carbamate

1.2 Other means of identification

Product number -
Other names diethyl N,N'-1,3-phenylenedicarbamate

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:7450-61-5 SDS

7450-61-5Relevant academic research and scientific papers

Nitration of ethyl carbamates of phenylenediamines and aniline

Davis, Matthew C.

, p. 2079 - 2089 (2008/02/04)

The methyl and ethyl carbamates of aniline and the diethyl dicarbamates of 1,2-, 1,3-, and 1,4-phenylenediamine were prepared. Nitration of the carbamates gave ring mono-, di-, or trinitro-derivatives in good yield. Copyright Taylor & Francis Group, LLC.

A new access to quinazolines from simple anilines

Chilin, Adriana,Marzaro, Giovanni,Zanatta, Samuele,Barbieri, Vera,Pastorini, Giovanni,Manzini, Paolo,Guiotto, Adriano

, p. 12351 - 12356 (2007/10/03)

A new synthetic pathway to quinazolines is described. This new method uses hexamethylenetetramine in TFA and potassium ferricyanide in aqueous ethanolic KOH, starting from simple N-protected anilines. The method affords substituted quinazolines with high

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