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4-methyl-2-vinyl-1,3-dioxane an is organic compound with the molecular formula C6H10O2. It is a colorless liquid with a fruity odor and is commonly used as a solvent, stabilizer, and intermediate in the synthesis of various chemicals. 4-methyl-2-vinyl-1,3-dioxane is characterized by its 1,3-dioxane ring structure, which consists of two oxygen atoms and three carbon atoms, with a methyl group attached to one of the carbons and a vinyl group on another carbon. Due to its unique structure, 4-methyl-2-vinyl-1,3-dioxane exhibits properties such as low toxicity, high boiling point, and good solubility in various solvents, making it a versatile chemical in the industry.

6542-56-9

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6542-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6542-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6542-56:
(6*6)+(5*5)+(4*4)+(3*2)+(2*5)+(1*6)=99
99 % 10 = 9
So 6542-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-7-8-5-4-6(2)9-7/h3,6-7H,1,4-5H2,2H3

6542-56-9SDS

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 2-ethenyl-4-methyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-Vinyl-4-methyl-1,3-dioxan

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:6542-56-9 SDS

6542-56-9Downstream Products

6542-56-9Relevant academic research and scientific papers

Synthesis of tetrahydrofuran

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, (2008/06/13)

This invention provides a process for producing tetrahydrofuran by the reaction of 3-(5'-alkyl-1',3'-dioxane)-propionaldehyde and/or 3-(5'-alkyl-1',3'-dioxane)propanol and/or 4-hydroxybutanal with hydrogen in an aqueous medium having a pH between about 0.1 and 5. Maintenance of the reaction medium within the specified acidic range of pH is an important feature of the invention process.

Preparation of an acetal from a diol and acrolein

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, (2008/06/13)

A process for preparing an acetal from acrolein and a 1,3-diol whereby substantially complete conversion of the acrolein to acetal is attained, by simultaneously reacting and separating by extraction the acetal and water formed from said diol and acrolein reaction, said process comprising continuously feeding a 1,3-diol and an acid catalyst countercurrent to a solvent while continuously feeding acrolein to the solvent and diol, separating the acetal-solvent from the diol-water, optionally separating the acetal and solvent and optionally separating the diol and water.

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