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Ethyl (2,4,6-trimethyl-1,3-dioxan-2-yl)acetate is a chemical compound with the molecular formula C10H18O4. It is a colorless liquid with a fruity odor and is commonly used as a synthetic flavoring agent in the food and beverage industry. ethyl (2,4,6-trimethyl-1,3-dioxan-2-yl)acetate is characterized by its 1,3-dioxane ring structure, which is substituted with three methyl groups at the 2, 4, and 6 positions, and an ethyl acetate group attached to the 2-position. It is known for its ability to impart a pleasant, fruity aroma to various products, making it a valuable component in the creation of artificial fruit flavors. The compound is also recognized for its stability and is often used in applications where a long shelf life is desired.

6472-11-3

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6472-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6472-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6472-11:
(6*6)+(5*4)+(4*7)+(3*2)+(2*1)+(1*1)=93
93 % 10 = 3
So 6472-11-3 is a valid CAS Registry Number.

6472-11-3SDS

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 ethyl 2-(2,4,6-trimethyl-1,3-dioxan-2-yl)acetate

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:6472-11-3 SDS

6472-11-3Downstream Products

6472-11-3Relevant academic research and scientific papers

New 2,4,6-substituted 1,3-dioxanes: Synthesis, stereochemistry and thermodynamic data determinations by cis-trans isomers equilibrium

Balog, Mirela,Ramondenc, Yvan,Oprean, Ioan,Grosu, Ion,Ple, Gerard

, p. 389 - 394 (2007/10/03)

The thermodynamic data (A-values) for some substituents located at position 2 of the 1,3-dioxane ring are calculated from the ratio (measured by GC-MS and NMR) of cis and trans isomers of some 2,4,6-substituted-1,3-dioxanes obtained by the condensation reaction of meso 2,4-pentanediol with several aldehydes and ketones. The stereochemistry of these compounds is deduced from high-field NMR experiments.

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