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2,4,6-trimethyl-1,3-dioxane is a cyclic ether chemical compound with the molecular formula C8H16O2. It is a colorless, flammable liquid at room temperature and is classified as a volatile organic compound. Due to its potential health risks when inhaled or absorbed through the skin, it is essential to handle this chemical with caution and follow proper safety measures.

19145-91-6

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19145-91-6 Usage

Uses

Used in Fragrance Production:
2,4,6-trimethyl-1,3-dioxane is used as a key component in the production of fragrances, contributing to the creation of various scents for personal care products, household items, and other applications.
Used in Industrial Solvents:
In various industries, 2,4,6-trimethyl-1,3-dioxane is used as a solvent, facilitating the dissolution of other substances in manufacturing processes. Its solvent properties make it a valuable component in the production of paints, coatings, and adhesives, among other products.

Check Digit Verification of cas no

The CAS Registry Mumber 19145-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19145-91:
(7*1)+(6*9)+(5*1)+(4*4)+(3*5)+(2*9)+(1*1)=116
116 % 10 = 6
So 19145-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-5-4-6(2)9-7(3)8-5/h5-7H,4H2,1-3H3

19145-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trimethyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names trans-2-methylcinnamoyl chloride

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:19145-91-6 SDS

19145-91-6Downstream Products

19145-91-6Relevant academic research and scientific papers

Stereoelectronic Control in the Gas-Phase Ionization of Cyclic Ortho Esters

Caserio, Marjorie C.,Souma, Yoshie,Kim, Jhong K.

, p. 6712 - 6716 (2007/10/02)

As a test of stereoelectronic control in the gas phase, the rates of ionic cleavage of the exocyclic methoxyl group of 2-methoxy-cis-4,6-dimethyl-1,3-dioxane diastereomers have been measured by ion cyclotron resonance techniques.The reactant ions were isopropyl and (methylthio)methyl cations derived from electron impact cleavage of 2-methylpropane and 2-(methylthio)ethanol, respectively.Within experimental error, the rates of cleavage of the equatorial methoxyl were the same as those of the axial methoxyl with a given reactant ion.With use of mixtures of deuterium-labeled and unlabeled diastereomers and reactant ions derived from isopropyl ether and acetylacetone, a slight (10percent) preference was seen for cleavage of the axial methoxyl group.The significance of these results in terms of stereoelectronic and conformational effects is discussed.

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