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1-Nitro-4-penta-1,3-dien-1-yl-benzene is a complex organic compound with the molecular formula C11H9NO2. It is a derivative of benzene, featuring a nitro group (-NO2) attached to the 1st carbon atom and a penta-1,3-dien-1-yl group (a conjugated diene system) attached to the 4th carbon atom. 1-nitro-4-penta-1,3ξ-dien-ξ-yl-benzene is characterized by its aromatic structure and the presence of a reactive nitro group, which can participate in various chemical reactions, such as reduction to an amine or participation in electrophilic aromatic substitution. The conjugated diene system in the side chain adds to the compound's reactivity and potential for further chemical transformations. Due to its complex structure, 1-nitro-4-penta-1,3-dien-1-yl-benzene may have applications in the synthesis of more complex organic molecules or as an intermediate in the production of certain pharmaceuticals or specialty chemicals.

3909-95-3

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3909-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3909-95-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3909-95:
(6*3)+(5*9)+(4*0)+(3*9)+(2*9)+(1*5)=113
113 % 10 = 3
So 3909-95-3 is a valid CAS Registry Number.

3909-95-3Downstream Products

3909-95-3Relevant articles and documents

Palladium-Catalyzed Syntheses of Aryl Polyenes

Mitsudo, Taki-aki,Fischetti, William,Heck, Richard F.

, p. 1640 - 1646 (2007/10/02)

The palladium-catalyzed arylation reaction has been employed to prepare a variety of mono- and diaryl 1,3-dienes and 1,3,5-trienes.The yields were good when electron withdrawing substituents were present in the aryl groups but only poor to fair when electron-donating groups were involved.Monoaryl dienes and trienes reacted well with all types of aryl halides to give mixed diaryl derivatives. 2-Bromostyrene reacts with phenylhexatriene to form 1,8-diphenyloctatetraene and with hexatriene to form 1,10-diphenyldecapentaene, but both only in about 15percent yield.

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