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2H-Pyran-2-one, tetrahydro-6-methylene-, also known as 6-methylene-tetrahydro-2H-pyran-2-one, is an organic compound with the molecular formula C6H8O2. It is a heterocyclic compound, specifically a pyrone derivative, which features a six-membered ring with one oxygen atom and a double bond between carbons 6 and 7. 2H-Pyran-2-one, tetrahydro-6-methylene- is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and natural products due to its unique structure and reactivity.

5636-66-8

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5636-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5636-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5636-66:
(6*5)+(5*6)+(4*3)+(3*6)+(2*6)+(1*6)=108
108 % 10 = 8
So 5636-66-8 is a valid CAS Registry Number.

5636-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (rac)-6-methylenetetrahydropyran-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5636-66-8 SDS

5636-66-8Relevant academic research and scientific papers

Metalloenzyme-mimicking supramolecular catalyst for highly active and selective intramolecular alkyne carboxylation

Lee, Li-Chen,Zhao, Yan

, p. 5579 - 5582 (2014/05/06)

Creation of synthetic catalysts with enzyme-like behavior is challenging despite strong interest in such systems. Extraction of tetrachloroaurate into the hydrophilic core of an interfacially cross-linked reverse micelle (ICRM) produced an artificial "metalloenzyme" with highly unusual catalytic properties. The ICRM pulled the substrate toward the catalytic metal, which converted it efficiently to the product that was rapidly ejected. These features enabled greatly reduced catalyst loading (30-100 times lower than typical levels used in literature examples), constant high reaction rate throughout the course of the reaction, lack of the hydrolyzed side product, and substrate selectivity unobserved in conventional gold catalysts.

Intramolecular cyclization of γ-acetylenic acids using dendrimer-encapsulated Pd2+ catalysts

Maeno, Zen,Mitsudome, Takato,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

, p. 947 - 954 (2013/08/15)

Polyamine dendrimer-encapsulated Pd2+ catalysts were prepared by complexation of PdCl2 with internal tertiary amino groups of the dendrimer. The fifth-generation Pd2+ dendrimer catalyst showed cooperative catalysis between Pd2+ species and the internal nanocavity consisting of regularly arranged tertiary amino groups to promote the intramolecular cyclization of γ-acetylenic acids efficiently.

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