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Z-1-(2-cyanophenyl)-2-cyanoethene is an organic compound characterized by its molecular formula C11H5N3. It is a derivative of ethene, featuring a cyanophenyl group and a cyano group attached to the double-bonded carbon atoms. This molecule is known for its conjugated system, which extends across the phenyl ring and the ethene moiety, contributing to its electronic properties. The compound is of interest in organic chemistry and materials science, potentially for its electronic and optical characteristics. It is important to note that due to the presence of cyano groups, which can release hydrogen cyanide under certain conditions, Z-1-(2-cyanophenyl)-2-cyanoethene should be handled with care due to its potential toxicity.

4508-50-3

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4508-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4508-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,0 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4508-50:
(6*4)+(5*5)+(4*0)+(3*8)+(2*5)+(1*0)=83
83 % 10 = 3
So 4508-50-3 is a valid CAS Registry Number.

4508-50-3Relevant academic research and scientific papers

Carbon-carbon cleavage of aryl diamines and quinone formation using sodium periodate: a novel application

Telvekar, Vikas N.,Takale, Balaram S.

, p. 3940 - 3943 (2010)

A first novel synthetic utility of sodium periodate for aryl diamine carbon-carbon cleavage is described. Aryl 1,2-diamine compounds were successfully converted into corresponding nitriles, while the developed method is also useful for the preparation of quinones from corresponding aryl 1,4-diamine compounds. The advantages of this protocol are shorter reaction time and mild reaction conditions to obtain moderate to good yields.

CUCN-MEDIATED ONE POT PRODUCTION OF CINNAMONITRILE DERIVATIVES

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Paragraph 0043; 0046 - 0048; 0057, (2015/02/19)

The present invention discloses a cheaper and practical protocol for the construction of a wide variety of o-cyanocin-namonitrile and their structural analogues that proceeds with good yields in a single step using CuCN as the only reagent.

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