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3,3,4-Triphenylbutan-2-one is an organic compound with the molecular formula C26H22O. It is a white crystalline solid that is soluble in organic solvents. 3,3,4-triphenylbutan-2-one is characterized by the presence of three phenyl groups attached to a butanone backbone, with the carbonyl group (C=O) located at the second carbon. It is synthesized through various chemical reactions, such as the Friedel-Crafts acylation of triphenylmethane with acetyl chloride. 3,3,4-Triphenylbutan-2-one has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

5350-79-8

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5350-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5350-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5350-79:
(6*5)+(5*3)+(4*5)+(3*0)+(2*7)+(1*9)=88
88 % 10 = 8
So 5350-79-8 is a valid CAS Registry Number.

5350-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4-triphenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 3,3,4-Triphenyl-butan-2-on

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:5350-79-8 SDS

5350-79-8Downstream Products

5350-79-8Relevant academic research and scientific papers

Pinacol Rearrangement and Direct Nucleophilic Substitution of Allylic Alcohols Promoted by Graphene Oxide and Graphene Oxide CO2H

Gómez-Martínez, Melania,Baeza, Alejandro,Alonso, Diego A.

, p. 1032 - 1039 (2017/03/27)

Graphene oxide (GO) and carboxylic acid functionalized GO (GO–CO2H) have been found to efficiently promote the heterogeneous and environmentally friendly pinacol rearrangement of 1,2-diols and the direct nucleophilic substitution of allylic alcohols. In general, high yields and regioselectivities are obtained in both reactions using 20 wt % of catalyst loading and mild reaction conditions.

A one-pot cross-pinacol coupling/rearrangement procedure

Scheffler, Ulf,Mahrwald, Rainer

, p. 1970 - 1975,6 (2012/12/12)

A new catalytic retro-pinacol/cross-pinacol reaction, followed by subsequent rearrangement or deoxygenation of the intermediately formed vicinal diols, is described. This operationally simple one-pot protocol allows isolation of geminal α,α-diphenyl ketones or 1,1-diphenyl alkenes with high yields and selectivities. Copyright

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