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4-(2-hydroxy-2,2-diphenylethyl)benzonitrile is a complex organic chemical compound with the molecular formula C21H17NO. It is a derivative of benzonitrile, featuring a phenylethyl group attached to the 4-position of the benzene ring. The phenylethyl group itself consists of a hydroxyl group and two phenyl rings, making it a diphenylethyl moiety. 4-(2-hydroxy-2,2-diphenylethyl)benzonitrile is characterized by its unique structure, which includes a hydroxyl group that can participate in hydrogen bonding and a nitrile group that can engage in various chemical reactions. It is typically synthesized through organic synthesis methods and may have potential applications in the fields of pharmaceuticals, materials science, or as an intermediate in the synthesis of other complex molecules.

10517-66-5

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10517-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10517-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10517-66:
(7*1)+(6*0)+(5*5)+(4*1)+(3*7)+(2*6)+(1*6)=75
75 % 10 = 5
So 10517-66-5 is a valid CAS Registry Number.

10517-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxy-2,2-diphenylethyl)benzonitrile

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

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More Details:10517-66-5 SDS

10517-66-5Downstream Products

10517-66-5Relevant academic research and scientific papers

Sunlight-Driven Synthesis of Triarylethylenes (TAEs) via Metal-Free Mizoroki–Heck-Type Coupling

Onuigbo, Louis,Raviola, Carlotta,Di Fonzo, Andrea,Protti, Stefano,Fagnoni, Maurizio

, p. 5297 - 5303 (2018/09/14)

A protocol for the preparation of substituted triarylethylenes (TAEs) was developed by using arylazo sulfones as substrates in the presence of 1,1-diarylethylenes. The process took place efficiently in the absence of any (photo)catalyst upon exposure of the reaction mixture to (simulated) sunlight.

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