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(Z)-1-bromo-2-(4-methylstyryl)benzene is an organic chemical compound characterized by a unique molecular structure. It features a benzene ring with a bromine atom attached at the 1-position and a 4-methylstyryl group at the 2-position. The 4-methylstyryl group itself consists of a styrene moiety (a vinylbenzene) with a methyl group attached to the para position of the benzene ring. (Z)-1-bromo-2-(4-methylstyryl)benzene is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single carbon-carbon single bond, allowing for interesting chemical reactivity and potential applications in organic synthesis. The (Z) configuration indicates the geometric arrangement of the double bonds, with the bromine and methyl groups on the same side of the molecule when viewed along the double bond axis. (Z)-1-bromo-2-(4-methylstyryl)benzene is a halogenated aromatic, which may have applications in the synthesis of pharmaceuticals, agrochemicals, or materials science due to its specific structural features.

4780-81-8

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4780-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4780-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,8 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4780-81:
(6*4)+(5*7)+(4*8)+(3*0)+(2*8)+(1*1)=108
108 % 10 = 8
So 4780-81-8 is a valid CAS Registry Number.

4780-81-8Relevant academic research and scientific papers

Polycyclic Aromatic Hydrocarbons via Iron(III)-Catalyzed Carbonyl-Olefin Metathesis

McAtee, Christopher C.,Riehl, Paul S.,Schindler, Corinna S.

supporting information, p. 2960 - 2963 (2017/03/11)

Polycyclic aromatic hydrocarbons are important structural motifs in organic chemistry, pharmaceutical chemistry, and materials science. The development of a new synthetic strategy toward these compounds is described based on the design principle of iron(III)-catalyzed carbonyl-olefin metathesis reactions. This approach is characterized by its operational simplicity, high functional group compatibility, and regioselectivity while relying on FeCl3 as an environmentally benign, earth-abundant metal catalyst. Experimental evidence for oxetanes as reactive intermediates in the catalytic carbonyl-olefin ring-closing metathesis has been obtained.

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