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Ethyl dipentylcarbamate is a chemical compound with the molecular formula C12H25NO2. It is an ester derivative of carbamic acid, where the hydroxyl group is replaced by an ethyl group and two pentyl groups are attached to the nitrogen atom. This organic compound is characterized by its oily liquid state and is insoluble in water. It is synthesized by reacting ethyl isocyanate with pentyl alcohol and is used in various applications, including as a solvent, a chemical intermediate, and potentially in the production of pharmaceuticals and agrochemicals. Due to its specific structure and properties, ethyl dipentylcarbamate may also be of interest in research and development for new materials and compounds.

5465-92-9

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5465-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5465-92-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5465-92:
(6*5)+(5*4)+(4*6)+(3*5)+(2*9)+(1*2)=109
109 % 10 = 9
So 5465-92-9 is a valid CAS Registry Number.

5465-92-9SDS

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,N-dipentylcarbamate

1.2 Other means of identification

Product number -
Other names ethyl dipentylcarbamate

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 -
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More Details:5465-92-9 SDS

5465-92-9Downstream Products

5465-92-9Relevant academic research and scientific papers

REACTION DES CHLOROFORMIATES SUR LES AMINES TERTIAIRES: COMPETITION ENTRE N-DEMETHYLATION, DESAMINATION, N-DEBENZYLATION ET N-DESALLYLATION

Kapnang, Henriette,Charles, Georges

, p. 3233 - 3236 (2007/10/02)

In ten cases investigated for the title reaction, N-debenzylation and N-deallylation are favoured over deamination and N-demethylation.

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