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Hexadecanoic acid, 3-oxo-1-cyclohexen-1-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116854-41-2

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116854-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116854-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,8,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116854-41:
(8*1)+(7*1)+(6*6)+(5*8)+(4*5)+(3*4)+(2*4)+(1*1)=132
132 % 10 = 2
So 116854-41-2 is a valid CAS Registry Number.

116854-41-2SDS

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 (3-oxocyclohexen-1-yl) hexadecanoate

1.2 Other means of identification

Product number -
Other names 3-palmitoyloxy-2-cyclohexene-1-one

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:116854-41-2 SDS

116854-41-2Relevant academic research and scientific papers

New fatty acid derivatives based on barbiturates and other cyclic β-dicarbonyl compounds and an acyl migration

Noroozi Pesyan, Nader,Bagheri, Marziyeh,Sahin, Ertan,Tunc, Tuncay

, p. 1429 - 1437 (2014/12/09)

The use of DCC, triethylamine and 4-dimethylaminopyridine in dichloromethane provides a general and standard one-pot procedure for the O-acylation of cyclic β-dicarbonyl compound derivatives (1) with palmitic and stearic acids which have long hydrocarbon tails, to synthesis of new type of fatty acid derivative in good to excellent yields. Structure elucidation was carried out by FT-IR, 1H NMR and 13C NMR spectroscopy techniques. The acyl migration was also found in results and the corresponding structure was characterized by X-ray crystallography. A proposed mechanism was discussed for the formation of products.

Synthesis of Lepidoptera Kairomones and Their Analogs, Derivatives of 2-Acylcyclohexane-1,3-Diones, with an Saturated Acyl Side Chain

Lakhvich, F. A.,Petrusevich, I. I.,Sergeeva, A. N.

, p. 1473 - 1479 (2007/10/03)

Preparative synthesis of natural 2-acylcyclohexane-1,3-diones and their structural analogs is performed by O-C isomerization of monoenol esters of cyclohexane-1,3-diones and saturated fatty acids under the action of aluminum chloride, sodium acetate, or d

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