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1-Methyl-2-oxatricyclo[3.3.1.13,7]decane is a complex organic compound with the molecular formula C10H15NO. It is a tricyclic structure, which means it consists of three interconnected rings. The compound features a methyl group (CH3) attached to one of the carbon atoms, and an oxygen atom that forms part of a heterocyclic ring, specifically a tricyclo structure with one oxygen atom and ten carbon atoms. This molecule is known for its unique structure and potential applications in various chemical and pharmaceutical processes. Due to its specific arrangement of atoms and functional groups, it can participate in a range of chemical reactions and may have properties that are of interest in the development of new drugs or other chemical products.

6508-22-1

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6508-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6508-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6508-22:
(6*6)+(5*5)+(4*0)+(3*8)+(2*2)+(1*2)=91
91 % 10 = 1
So 6508-22-1 is a valid CAS Registry Number.

6508-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-oxa-adamantane

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-oxo-adamantan

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:6508-22-1 SDS

6508-22-1Downstream Products

6508-22-1Relevant academic research and scientific papers

Chemo-Selectivity of Group-VIII Metal Catalysts in Hydrogenation of Nonconjugated Enones

Ishiyama, Jun-ichi,Maeda, Satoshi,Takahashi, Kazuhiro,Senda, Yasuhisa,Imaizumi, Shin

, p. 1721 - 1726 (2007/10/02)

The chemo-selectivity of group-VIII metal catalysts has been examined in the hydrogenation of nonconjugated enones at ambient temperature under an atmospheric pressure of hydrogen.A cobalt catalyst gave high yields of unsaturated alcohols from trialkylated olefinic ketones.Osmium showed the highest selectivity among platinum metal catalysts for the reduction of the carbonyl bond in the hydrogenation of trialkylated olefinic ketones.The hydrogenation of mono- and dialkylated olefinic ketone ordinarily proceeded with a preferential saturation of the olefinic function, regardless of the catalysts.The hydrogenation of 4-methylene- and 4-ethylidenecyclohexanone was accompanied by the formation of diethyl acetals over ruthenium, rhodium, and palladium black catalysts in an ethanol solvent.The acetals were not detected in the hydrogenation of the other enones and over the other catalysts.In addition, the chemoselectivity on the hydrogenation of acyclic enones was examined over nickel and cobalt catalysts treated with small amounts of alkali and carbon monoxide.The amount of unsaturated alcohols increased when the catalyst was treated with alkali in the case of di- and trialkylated olefinic ketones, whereas the characteristics of cobalt, which selectively reduces the ketonic function in trialkylated olefinic ketoones, were completely missing when cobalt was treated with carbon monoxide.

HYDROGENATION OF 7-METHYLENEBICYCLONONAN-3-ONE OVER GROUP VIII METAL CATALYSTS. NOVEL REDUCTIVE CYCLIZATION

Ishiyama, Jun-ichi,Senda, Yasuhisa,Imaizumi, Shin

, p. 771 - 774 (2007/10/02)

The products of novel reductive cyclization, 1-adamantanol and 1-methyl-2-oxa-adamantane, were obtained in the hydrogenation of 7-methylenebicyclononan-3-one over group VIII metal black catalysts in ethanol or cyclohexane. 1-Adamantanol was produced over Pd, Rh, Co and Ni catalysts, and 1-methyl-2-oxa-adamantane only over Co catalysts in cyclohexane.

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