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N,N-dimethyl-N-(2'-methylphenyl)amine N-oxide, also known as DMP-30, is an organic compound with the chemical formula C9H14N2O. It is a derivative of N,N-dimethylaniline, featuring a methyl group attached to the phenyl ring at the 2' position and an N-oxide functional group. N,N-dimethyl-N-(2'-methylphenyl)amine N-oxide is a colorless to pale yellow liquid with a characteristic amine-like odor. It is used as a polymerization inhibitor, particularly in the production of polypropylene and other olefin polymers, to prevent unwanted side reactions and control the molecular weight of the polymer. DMP-30 is also known for its effectiveness in protecting against thermal and oxidative degradation, ensuring the stability and quality of the final polymer product.

6852-47-7

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6852-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6852-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6852-47:
(6*6)+(5*8)+(4*5)+(3*2)+(2*4)+(1*7)=117
117 % 10 = 7
So 6852-47-7 is a valid CAS Registry Number.

6852-47-7Relevant academic research and scientific papers

Synthesis of Halogenated Anilines by Treatment of N, N-Dialkylaniline N-Oxides with Thionyl Halides

Reed, Hayley,Paul, Tyler R.,Chain, William J.

, p. 11359 - 11368 (2018/08/06)

The special reactivity of N,N-dialkylaniline N-oxides allows practical and convenient access to electron-rich aryl halides. A complementary pair of reaction protocols allow for the selective para-bromination or ortho-chlorination of N,N-dialkylanilines in up to 69% isolated yield. The generation of a diverse array of halogenated anilines is made possible by a temporary oxidation level increase of N,N-dialkylanilines to the corresponding N,N-dialkylaniline N-oxides and the excision of the resultant weak N-O bond via treatment with thionyl bromide or thionyl chloride at low temperature.

Catalytic N-oxidation of tertiary amines on RuO2NPs anchored graphene nanoplatelets

Gopiraman, Mayakrishnan,Bang, Hyunsik,Babu, Sundaram Ganesh,Wei, Kai,Karvembu, Ramasamy,Kim, Ick Soo

, p. 2099 - 2106 (2014/06/24)

Ultrafine ruthenium oxide nanoparticles (RuO2NPs) with an average diameter of 1.3 nm were anchored on graphene nanoplatelets (GNPs) using a Ru(acac)3 precursor by a very simple dry synthesis method. The resultant material (GNPs-RuO2NPs) was used as a heterogeneous catalyst for the N-oxidation of tertiary amines for the first time. The transmission electron microscopy (TEM) images of the GNPs-RuO2NPs showed the excellent attachment of RuO2NPs on GNPs. The loading of Ru in GNPs-RuO2NPs was 2.68 wt%, as confirmed by scanning electron microscope-energy dispersive spectroscopy (SEM-EDS). The X-ray photoelectron spectrum (XPS) and the X-ray diffraction pattern (XRD) of GNPs-RuO 2NPs revealed that the chemical state of Ru on GNPs was +4. After the optimization of reaction conditions for N-oxidation of triethylamine, the scope of the reaction was extended to various aliphatic, alicyclic and aromatic tertiary amines. The GNPs-RuO2NPs showed excellent catalytic activity in terms of yields even at a very low amount of Ru catalyst (0.13 mol%). The GNPs-RuO2NPs was heterogeneous in nature, chemically as well as physically, very stable and could be reused up to 5 times. The Royal Society of Chemistry 2014.

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