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α-Bromoacetyl-β-dimethylamino-2-nitrostyrene is a complex organic chemical compound characterized by its unique molecular structure. It features a nitro group (NO2) attached to the 2-position of a styrene backbone, which is a phenyl ring (C6H5) linked to an ethylene group (CH=CH2). The α-position of the acetyl group (CH3CO) is brominated (Br), while the β-position is substituted with a dimethylamino group (N(CH3)2). α-bromoacetyl-β-dimethylamino-2-nitrostyrene is known for its potential applications in the synthesis of various pharmaceuticals and dyes due to its reactive functional groups, which can participate in a range of chemical reactions. Its molecular formula is C11H12BrNO3, and it has a molecular weight of 290.13 g/mol. The compound's properties, such as its reactivity and solubility, make it a valuable intermediate in organic synthesis, particularly in the preparation of compounds with potential biological activity.

58678-89-0

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58678-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58678-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,7 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58678-89:
(7*5)+(6*8)+(5*6)+(4*7)+(3*8)+(2*8)+(1*9)=190
190 % 10 = 0
So 58678-89-0 is a valid CAS Registry Number.

58678-89-0Relevant academic research and scientific papers

Process for preparing o-nitrobenzylketones

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, (2008/06/13)

o-nitrobenzylketones are prepared by reacting a trans-β-substituted amino-2-nitrostyrene with a lower alkanoyl halide, halo-lower alkanoyl halide, phthalimido-lower alkanoyl halide, benzoyl halide or substituted benzoyl halide, and subsequently hydrolyzing the resulting product to yield the desired o-nitrobenzylketone.

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