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methyl 2-tetradecylglycidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69207-52-9

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69207-52-9 Usage

Uses

Different sources of media describe the Uses of 69207-52-9 differently. You can refer to the following data:
1. Antidiabetic.
2. Methyl Palmoxirate is an inhibitor of fatty acid oxidation.

Check Digit Verification of cas no

The CAS Registry Mumber 69207-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69207-52:
(7*6)+(6*9)+(5*2)+(4*0)+(3*7)+(2*5)+(1*2)=139
139 % 10 = 9
So 69207-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18(16-21-18)17(19)20-2/h3-16H2,1-2H3

69207-52-9SDS

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 Methyl palmoxirate

1.2 Other means of identification

Product number -
Other names methyl 2-tetradecyloxirane-2-carboxylate

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:69207-52-9 SDS

69207-52-9Downstream Products

69207-52-9Relevant academic research and scientific papers

The Baylis-Hillman chemistry in aqueous media: A convenient synthesis of 2-methylenealkanoates and alkanenitriles

Basavaiah, Deevi,Kumaragurubaran, Nagaswamy

, p. 477 - 479 (2007/10/03)

A convenient, general and efficient synthesis of 2-methylenealkanoates and alkanenitriles is accomplished via the regioselective nucleophilic (SN2′) addition of hydride ion from NaBH4 to (2Z)-2-(bromomethyl)alk-2-enoates and 2-(bromomethyl)alk-2-enenitriles respectively in the presence of DABCO in environment friendly aqueous media. Synthesis of two hypoglycemic agents is also described.

Alkylglycidic Acids: Potential New Hypoglycemic Agents

Ho, Winston,Tutwiler, Gene F.,Cottrell, Sandra C.,Morgans, Dave J.,Tarhan, Okan,Mohrbacher, Richard J.

, p. 2184 - 2190 (2007/10/02)

A series of alkylglycidic acid analogues and derivatives were synthesized and tested for their ability to inhibit long-chain fatty acid oxidation in vitro and to lower blood sugar in rats.The extent of inhibition of carnitine acyl transferase, the enzyme

Process for production of methyl 2-tetradecylgycidate

-

, (2008/06/13)

An improved process for producing the hypoglycemic compound, methyl 2-tetradecylglycidate, by reacting methyl α-chloropalmitate with lithium methoxide in the presence of formaldehyde in a dipolar aprotic solvent such as DMF or DMSO.

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