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Ethyl (naphthalen-1-ylmethyl)carbamate is a chemical compound with the molecular formula C13H15NO2. It is a derivative of naphthalene, an aromatic hydrocarbon, and is characterized by the presence of a carbamate functional group. ethyl (naphthalen-1-ylmethyl)carbamate is known for its potential use as an insecticide, particularly in the control of certain pests due to its ability to disrupt the nervous system of insects. The structure of ethyl (naphthalen-1-ylmethyl)carbamate features a naphthalene ring attached to a methylene group, which in turn is connected to an ethyl carbamate group. Its chemical properties and potential applications make it a subject of interest in the field of agrochemicals and pest management.

4096-83-7

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4096-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4096-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4096-83:
(6*4)+(5*0)+(4*9)+(3*6)+(2*8)+(1*3)=97
97 % 10 = 7
So 4096-83-7 is a valid CAS Registry Number.

4096-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(naphthalen-1-ylmethyl)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

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More Details:4096-83-7 SDS

4096-83-7Downstream Products

4096-83-7Relevant academic research and scientific papers

The synthesis of alkyl carbamates from primary aliphatic amines and dialkyl carbonates in supercritical carbon dioxide

Selva, Maurizio,Tundo, Pietro,Perosa, Alvise

, p. 1217 - 1219 (2002)

At 130°C and in the presence of compressed CO2, primary aliphatic amines [RNH2, R=C10H21, C8H17, cHex, 1-(C10H7)CH2] react with organic carbonates (R′OCOsu

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