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Cis-4,4'-dicyanostilbene is an organic compound with the chemical formula C16H10N2. It is a derivative of stilbene, featuring two nitrile groups (CN) attached to the para positions of the benzene rings. This molecule exhibits a cis configuration, meaning the nitrile groups are positioned on the same side of the double bond connecting the benzene rings. Cis-4,4'-dicyanostilbene is known for its electronic properties and potential applications in materials science, such as in the development of organic semiconductors and conductive polymers. Its unique structure allows for interesting photophysical and electronic behavior, making it a subject of interest in chemical research.

2510-73-8

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2510-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2510-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2510-73:
(6*2)+(5*5)+(4*1)+(3*0)+(2*7)+(1*3)=58
58 % 10 = 8
So 2510-73-8 is a valid CAS Registry Number.

2510-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Bis(4-ethoxyphenyl)-1,2-ethanedione

1.2 Other means of identification

Product number -
Other names cis-Stilbene

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:2510-73-8 SDS

2510-73-8Relevant academic research and scientific papers

Enantioselective ring-opening reaction of meso-epoxides with ArSH catalyzed by a C2-symmetric chiral bipyridyldiol-titanium complex

Chen, Yi-Jing,Chen, Chinpiao

, p. 1313 - 1319 (2008/02/09)

This study describes a C2-symmetric ligand comprising a central bipyridine-pinene-derived core and two functionalized diphenylmethanol subunits. [8′-(Hydroxy-diphenyl-methyl)-10,10,10′,10′-tetramethy l-[5,5′]bi[6-aza-tricyclo[7.1.1.02,7/s

Crown ether catalyzed stereospecific synthesis of Z- and E-stilbenes by Wittig reaction in a solid-liquid two-phases system

Bellucci, Giuseppe,Chiappe, Cinzia,Lo Moro, Giacomo

, p. 4225 - 4228 (2007/10/03)

Potassium hydroxide and a catalytic amount of 18-crown-6 are used, in alternative to the classical Wittig conditions, to prepare very rapidly and stereoselectively Z- and E-stilbenes. In particular, the use of benzyltriphenylphosphonium iodides always leads to a complete Z- stereospecificity, while benzyldiphenylchlorophosphonium salts give a complete E-stereospecificity.

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