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Ethyl 6-oxodecanoate, also known as ethyl pelargonate, is a colorless liquid organic compound with the chemical formula C10H18O3. It is an ester derived from the carboxylic acid 6-oxodecanoic acid and ethanol. ETHYL 6-OXODECANOATE is characterized by its fruity, apple-like odor and is commonly used in the fragrance industry as a flavoring agent and perfume ingredient. Ethyl 6-oxodecanoate is also employed in the synthesis of various chemicals and pharmaceuticals, owing to its versatile chemical properties. It is important to note that, like many chemicals, ethyl 6-oxodecanoate should be handled with care due to its potential irritant properties.

4144-61-0

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4144-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4144-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4144-61:
(6*4)+(5*1)+(4*4)+(3*4)+(2*6)+(1*1)=70
70 % 10 = 0
So 4144-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O3/c1-3-5-8-11(13)9-6-7-10-12(14)15-4-2/h3-10H2,1-2H3

4144-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 6-OXODECANOATE

1.2 Other means of identification

Product number -
Other names Decanoic acid,6-oxo-,ethyl ester

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:4144-61-0 SDS

4144-61-0Relevant academic research and scientific papers

A CONVENIENT METHOD FOR THE DIRECT PREPARATION OF KETONES FROM 2-(6-(2-METHOXYETHYL)PYRIDYL) CARBOXYLATES AND ALKYL IODIDES BY USE OF ZINC DUST AND A CATALYTIC AMOUNT OF NICKEL DICHLORIDE

Onaka, Makoto,Matsuoka, Yoshio,Mukaiyama, Teruaki

, p. 531 - 534 (2007/10/02)

Treatment of 2-(6-(2-methoxyethyl)pyridyl) carboxylates with alkyl iodides in the presence of zinc dust and a catalytic amount of NiCl2 in DMF at 50 deg C affords unsymmetrical ketones in good yields by a one-pot procedure.

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