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2,3-diethoxy-2,3-diphenyl-1,4-dioxane is a colorless liquid chemical compound belonging to the dioxane family, with a molecular formula of C18H22O4. It is synthesized through the reaction of phenylmagnesium bromide and diethyl carbonate. 2,3-diethoxy-2,3-diphenyl-1,4-dioxane has low solubility in water but is soluble in organic solvents such as ethanol, ether, and chloroform. Due to its potential harmful effects if inhaled, swallowed, or comes into contact with the skin, it requires careful handling.

6963-19-5

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6963-19-5 Usage

Uses

Used in Pharmaceutical Industry:
2,3-diethoxy-2,3-diphenyl-1,4-dioxane is used as a solvent for various pharmaceutical applications, facilitating the dissolution and stability of active pharmaceutical ingredients. Its solubility in organic solvents makes it suitable for use in the formulation of medications.
Used in Cosmetic Industry:
In the cosmetic industry, 2,3-diethoxy-2,3-diphenyl-1,4-dioxane serves as a solvent, aiding in the formulation of cosmetic products by enhancing the solubility of various ingredients. Its properties contribute to the stability and effectiveness of cosmetic formulations.
Used as a Reagent in Organic Synthesis:
2,3-diethoxy-2,3-diphenyl-1,4-dioxane is utilized as a reagent in organic synthesis, playing a crucial role in various chemical reactions. Its unique structure allows it to participate in a range of synthetic processes, contributing to the production of diverse organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 6963-19-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6963-19:
(6*6)+(5*9)+(4*6)+(3*3)+(2*1)+(1*9)=125
125 % 10 = 5
So 6963-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O4/c1-3-21-19(17-11-7-5-8-12-17)20(22-4-2,24-16-15-23-19)18-13-9-6-10-14-18/h5-14H,3-4,15-16H2,1-2H3

6963-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diethoxy-2,3-diphenyl-1,4-dioxane

1.2 Other means of identification

Product number -
Other names 2,3-diethoxy-2,3-diphenyldioxane

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:6963-19-5 SDS

6963-19-5Downstream Products

6963-19-5Relevant academic research and scientific papers

ELECTRON-TRANSFER OXIDATION OF DIOXENES. AN EXAMPLE OF RADICAL CATION DISPROPORTIONATION

Ciminale, Francesco,Lopez, Luigi

, p. 789 - 792 (2007/10/02)

Tris(p-bromophenyl ammoniumyl) tetrafluoroborate induces an easy electron-transfer process on dioxenes leading quantitatively to the corresponding α-diketones.A mechanism involving the disproportionation of the intermediate radical cations is discussed.

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