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1-Chloro-4-(dinitromethyl)benzene is an organic compound with the molecular formula C7H4ClN2O4. It is a derivative of benzene, where one hydrogen atom is replaced by a chlorine atom, and another hydrogen atom is replaced by a dinitromethyl group (-CH(NO2)2). 1-chloro-4-(dinitromethyl)benzene is characterized by its yellow crystalline appearance and has a molecular weight of 230.57 g/mol. It is an important intermediate in the synthesis of various pharmaceuticals, dyes, and other chemical products. Due to its reactive nature, it is typically handled with care in a controlled environment to prevent potential hazards.

7304-76-9

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7304-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7304-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7304-76:
(6*7)+(5*3)+(4*0)+(3*4)+(2*7)+(1*6)=89
89 % 10 = 9
So 7304-76-9 is a valid CAS Registry Number.

7304-76-9Downstream Products

7304-76-9Relevant academic research and scientific papers

Selective oxidative deoximation with anhydrous Ce(IV) sulfate

Asutay, Oktay,Hamarat, Nilüfer,Uludag, Nesimi,Co?kun, Necdet

, p. 3902 - 3904 (2015)

Anhydrous Ce(SO4)2 in chloroform selectively converts oximes into the parent carbonyl compounds in good yields. Hammett correlations helped to indicate a plausible mechanism for the above reaction. The formation of 1-(dinitromethyl)benzene was assumed to be a product of isonitroso hydrogen reaction with arylaldoximes.

Synthesis and Properties of Dinitromethylated Arenes. Reinvestigation of the Ponzio Reaction

Suzuku, Hitomi,Takaoka, Hiroshi,Yamamoto, Hidetoshi,Ogawa, Takuji

, p. 2927 - 2932 (2007/10/02)

Several title compounds have been prepared by the modified Ponzio procedure and their IR, 1 H and 13 C NMR data are presented.In some cases trinitromethylated arenes were obtained as a by-product.Oxidative cleavage to parent aldehydes and oxidation to carboxylic acids were the major competing reactions. 9-Anthracenecarbaldehyde oxime and 10-methyl-9-anthracenecarbaldehyde oxime reacted with nitrogen dioxide in an unexpected way, giving 10-nitro-9-anthracenecarbonitrile oxide and 10-methyl-10-nitro-9-anthrone as the respective main products.Nitration of (dinitromethyl)benzene has also been examined under various conditions.

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