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α,β-Dimethyl-p-nitro-styrol, also known as 4-nitro-α,β-dimethylstyrene, is an organic compound characterized by a nitro group (-NO2) attached to the para position of a styrene molecule, which is a derivative of benzene with a vinyl group (C=CH2). The α,β positions refer to the carbon atoms adjacent to the double bond in the vinyl group, with two methyl groups (-CH3) attached to these positions. α.β-Dimethyl-p-nitro-styrol is a yellowish liquid with a molecular formula of C10H11NO2 and a molecular weight of 177.20 g/mol. It is used in the synthesis of various chemicals and pharmaceuticals, and its properties include reactivity towards nucleophiles due to the electron-withdrawing effect of the nitro group, which can influence its chemical behavior in reactions.

18755-62-9

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18755-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18755-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,5 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18755-62:
(7*1)+(6*8)+(5*7)+(4*5)+(3*5)+(2*6)+(1*2)=139
139 % 10 = 9
So 18755-62-9 is a valid CAS Registry Number.

18755-62-9Downstream Products

18755-62-9Relevant academic research and scientific papers

Intermolecular Carbonyl–olefin Metathesis with Vinyl Ethers Catalyzed by Homogeneous and Solid Acids in Flow

Cerón-Carrasco, José Pedro,Leyva-Pérez, Antonio,Pérez-Sánchez, Horacio,Rivero-Crespo, Miguel ángel,Tejeda-Serrano, María

, p. 3846 - 3849 (2020)

The carbonyl–olefin metathesis reaction has experienced significant advances in the last seven years with new catalysts and reaction protocols. However, most of these procedures involve soluble catalysts for intramolecular reactions in batch. Herein, we show that recoverable, inexpensive, easy to handle, non-toxic, and widely available simple solid acids, such as the aluminosilicate montmorillonite, can catalyze the intermolecular carbonyl–olefin metathesis of aromatic ketones and aldehydes with vinyl ethers in-flow, to give alkenes with complete trans stereoselectivity on multi-gram scale and high yields. Experimental and computational data support a mechanism based on a carbocation-induced Grob fragmentation. These results open the way for the industrial implementation of carbonyl–olefin metathesis over solid catalysts in continuous mode, which is still the origin and main application of the parent alkene–alkene cross-metathesis.

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