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1,4-Dioxane, 2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24407-16-7

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24407-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24407-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24407-16:
(7*2)+(6*4)+(5*4)+(4*0)+(3*7)+(2*1)+(1*6)=87
87 % 10 = 7
So 24407-16-7 is a valid CAS Registry Number.

24407-16-7SDS

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 2,5-diphenyl-1,4-dioxane

1.2 Other means of identification

Product number -
Other names 1,4-Dioxane,2,5-diphenyl

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:24407-16-7 SDS

24407-16-7Upstream product

24407-16-7Relevant academic research and scientific papers

Clay Catalized Rearrangement of Phenyloxiranes

Martinez, Roberte,Velasco, Micaela,Martinez, Ignacio,Menconi, Italo,Ramirez, Alberto,Angeles, Enrique,Regla, Ignacio,Lopez, Rafael

, p. 1865 - 1866 (2007/10/03)

The reaction of phenyloxiranes with a clay produces aldehydes, ketones and cyclic ethers. This method has the advantage that experimental conditions are simple and the reagents used are cheaper.

Catalytic Hydrogenation of Styrene Oxide with Cationic Rhodium Complexes

Fujitsu, Hiroshi,Shirahama, Shinichi,Matsumura, Eiichi,Takeshita, Kenjiro,Mochida, Isao

, p. 2287 - 2290 (2007/10/02)

Catalytic hydrogenation of styrene oxide with cationic rhodium complexes was investigated to develop its selective conversion into the specific alcohol. β-Phenylethyl alcohol and phenylacetaldehyde were rather selectively produced without either α-phenylethyl alcohol or acetophenone through a selective antinormal fission of the epoxide ring.The catalytic activity and selectivity were found to depend strongly on the ligand, the activity for the formation of alcohol decreasing in the order, PEt3 > PMe3 PPh3 >> diphos.The highest yield, achieved by the PEt3 complex, reached as high as 82percent after 8 h of reaction.A possible mechanism was proposed to explain the selective formation of β-phenylethyl alcohol and the role of water as a cocatalyst in the catalytic hydrogenation.

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