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2-Ethyl-2,4,6-trimethyl-1,3-dioxane is an organic compound with the molecular formula C?H??O?. It is a cyclic ether consisting of a 1,3-dioxane ring, which is a six-membered ring containing two oxygen atoms. The molecule has an ethyl group (-CH?CH?) attached to the 2-position and three methyl groups (-CH?) at the 2, 4, and 6 positions. This chemical is primarily used as a solvent and a stabilizer in various industrial applications, such as in the production of polymers and resins. Due to its chemical structure, it exhibits low polarity and high boiling point, making it suitable for use in a range of chemical processes. However, it is important to handle 2-ethyl-2,4,6-trimethyl-1,3-dioxane with care, as it may have potential health and environmental risks.

6413-37-2

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6413-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6413-37-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6413-37:
(6*6)+(5*4)+(4*1)+(3*3)+(2*3)+(1*7)=82
82 % 10 = 2
So 6413-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O2/c1-5-9(4)10-7(2)6-8(3)11-9/h7-8H,5-6H2,1-4H3

6413-37-2SDS

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 2-ethyl-2,4,6-trimethyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-Aethyl-r-2,t-4,t-6-trimethyl-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:6413-37-2 SDS

6413-37-2Upstream product

6413-37-2Downstream Products

6413-37-2Relevant academic research and scientific papers

Process for the selective oxidation of alcohols using readily removable nitroxyl radicals

-

, (2008/06/13)

The invention relates to a process for the selective oxidation of alcohols to ketones or to aldehydes by means of an alkali hypohalite under alkaline conditions, which comprises carrying out the oxidation in the presence of a heterogeneous oxidation catalyst that is insoluble in the reaction medium and is selected from the group comprising the compounds of formula (I) (III), wherein n is a number from 3 to 3000; or a 4-oxy-2,2,6,6-tetramethylpiperidin-1-oxyl that is 4-oxy-bound to a Merrifield polymer. The invention relates also to the compounds of formulae (II) and (III) and to the use of the above-mentioned oxidation catalysts for the oxidation of alcohols.

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