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α-Chloro-β,β-dimethyl-p-nitrostyrene is an organic chemical compound characterized by its unique molecular structure. It features a nitro group (-NO2) attached to the para position of a styrene backbone, which is a vinylbenzene structure. The α position is occupied by a chlorine atom (-Cl), and the β position has two methyl groups (-CH3) attached to it. α-chloro-β,β-dimethyl-p-nitrostyrene is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactive sites and functional groups. It is also recognized for its reactivity and can be used as an intermediate in the production of more complex organic molecules. The compound's properties, such as its reactivity with nucleophiles and its potential to undergo elimination reactions, make it a valuable building block in organic synthesis.

69240-36-4

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69240-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69240-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69240-36:
(7*6)+(6*9)+(5*2)+(4*4)+(3*0)+(2*3)+(1*6)=134
134 % 10 = 4
So 69240-36-4 is a valid CAS Registry Number.

69240-36-4Downstream Products

69240-36-4Relevant academic research and scientific papers

Kinetics and Stereochemistry of Elimination of Nitrous Acid from 1-p-Nitrophenyl-2-nitroethyl Derivatives

Norris, Robert K.,Wright, Timothy A.

, p. 281 - 294 (2007/10/02)

The eliminations of nitrous acids from the compounds (1) and (6) are E2 processes, which proceed with a large primary kinetic isotope effect and with antiperiplanar stereochemistry.The rate of elimination of HNO2 fom (1) is intermediate between the rate o

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