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19780-16-6

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19780-16-6 Usage

General Description

1,2-Epoxyeicosane is a chemical compound that belongs to the class of epoxides, which are important intermediates in the synthesis of various compounds. It is a natural epoxy fatty acid and is derived from eicosane, a hydrocarbon found in the waxes of some plants. 1,2-Epoxyeicosane has been identified as a bioactive lipid with potential anti-inflammatory and anti-tumor properties. It has also been suggested to have potential therapeutic effects in the treatment of various diseases. Additionally, 1,2-Epoxyeicosane has been shown to play a role in cellular signaling and regulation of gene expression. Overall, 1,2-Epoxyeicosane is a biologically active compound with potential significance in various physiological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 19780-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19780-16:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*1)+(1*6)=136
136 % 10 = 6
So 19780-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-19-21-20/h20H,2-19H2,1H3

19780-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-octadecyloxirane

1.2 Other means of identification

Product number -
Other names 1,2-epoxyicosane

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:19780-16-6 SDS

19780-16-6Upstream product

19780-16-6Relevant articles and documents

Synthesis and unique catalytic performance of single-site Ti-containing hierarchical macroporous silica with mesoporous frameworks

Kamegawa, Takashi,Suzuki, Norihiko,Che, Michel,Yamashita, Hiromi

, p. 2873 - 2879 (2011)

Single-site Ti-containing hierarchical macroporous silica with mesoporous frameworks (Ti-MMS) was successfully prepared by a solvent evaporation method using organic surfactant and poly(methyl methacrylate) (PMMA) colloidal crystals as the template. The formation of a well-defined macroporous structure composed of mesoporous silica walls was characterized by SEM and TEM observations. The successful incorporation of tetrahedrally coordinated Ti oxide moieties within their frameworks was also confirmed by spectroscopic techniques such as UV-vis and XAFS measurements. Comparative studies revealed that Ti-MMS exhibited higher catalytic activities for the epoxidation of linear α-olefin compared to Ti-containing mesoporous silica without macropores (Ti-MS). The reaction rate was significantly enhanced on Ti-MMS depending on increases in the alkyl chain length of linear α-olefins. It was also found that Ti-MMS showed good catalytic performance in the selective epoxidation of methyl oleate, which is a kind of unsaturated fatty acid methyl ester (FAME), under acid-free reaction conditions with tert-butylhydroperoxide (TBHP) because of the advantages of the combination of hierarchical macroporous and mesoporous structures.

Palladium- and light-enhanced ring-opening of oxiranes by copper chloride

Muzart, Jacques,Riahi, Abdelkhalek

, p. 323 - 336 (2007/10/02)

The yields of chlorohydrins formed by cleavage of epoxides by CuCl2 is increased in the presence of small amounts of PdCl2(MeCN)2.The conversion drops dramatically on carrying out the reaction in the dark.The regiochemistry of the ring-opening is sensitive to the nature of the substituents.

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