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2-Hexanone, 6,6-dimethoxy-, also known as 6,6-dimethoxyhexan-2-one, is an organic compound with the chemical formula C8H16O3. It is a colorless liquid with a molecular weight of 160.21 g/mol. This ketone derivative features a six-carbon chain with a ketone group at the second carbon and two methoxy groups attached to the sixth carbon. It is used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and fragrances. Due to its low solubility in water and high solubility in organic solvents, it is often employed in the synthesis of complex organic molecules. The compound is also known for its potential applications in the field of materials science, particularly in the development of new polymers and coatings.

36727-63-6

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36727-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36727-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,2 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36727-63:
(7*3)+(6*6)+(5*7)+(4*2)+(3*7)+(2*6)+(1*3)=136
136 % 10 = 6
So 36727-63-6 is a valid CAS Registry Number.

36727-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethoxy-5-oxo-hexane

1.2 Other means of identification

Product number -
Other names 1,1-Dimethoxy-5-oxohexane

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:36727-63-6 SDS

36727-63-6Relevant academic research and scientific papers

Acid-catalyzed reactions of six- and seven-membered cyclic hemiperacetals and peracetals and of related bicyclic ozonides

Griesbaum, Karl,Kiesel, Gilbert,Mertens, Henri,Krieger-Beck, Petra,Henke, Henning

, p. 2198 - 2204 (2007/10/02)

HCl-catalyzed reactions of the hemiperacetals 3-methoxy-3-methyl-7-hydroxy-1,2-dioxepane (1a) and 3-methoxy-3-methyl-6-hydroxy-1,2-dioxane (1b) and of the related ozonides 1-methyl-6,7,8-trioxabicyclooctane (2a) and 1-methyl-5,6,7-trioxabicycloheptane (2b) gave peroxidic monocyclic (11-13), bicyclic (14), and (or) tricyclic (15) products.By contrast, reactions of the peracetals corresponding to 1a and 1b, viz., 3-methyl-3,7-dimethoxy-1,2-dioxepane (13a) and 3-methyl-3,6-dimethoxy-1,2-dioxane (13b) gave only non-peroxide products.Reactions of the persubstituted peracetals 3,6-dimethoxy-3,6-dimethyl-1,2-dioxane (25) and 3,6-dimethoxy-3-isopropyl-6-methyl-1,2-dioxane (27) also gave non-peroxidic products, which resulted from fragmentation of the carbon skeletons.

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