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2-methyl-1-phenyl-3-(o-tolyl)propan-1-one is an organic compound with the molecular formula C17H18O. It is a derivative of propanone, featuring a methyl group at the 2nd carbon, a phenyl group at the 1st carbon, and an o-tolyl group (ortho-methylphenyl) at the 3rd carbon. 2-methyl-1-phenyl-3-(o-tolyl)propan-1-one is characterized by its unique structure, which combines the properties of a ketone with the aromatic nature of the phenyl and o-tolyl groups. It is a colorless to pale yellow solid with a distinct aromatic odor. Due to its complex structure, it has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's chemical properties, such as reactivity and stability, are influenced by the presence of the phenyl and o-tolyl groups, making it an interesting subject for further research and development in the field of organic chemistry.

891-53-2

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891-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 891-53-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 891-53:
(5*8)+(4*9)+(3*1)+(2*5)+(1*3)=92
92 % 10 = 2
So 891-53-2 is a valid CAS Registry Number.

891-53-2Relevant academic research and scientific papers

Palladium-Catalyzed Synthesis of α-Methyl Ketones from Allylic Alcohols and Methanol

Biswal, Priyabrata,Samser, Shaikh,Meher, Sushanta Kumar,Chandrasekhar, Vadapalli,Venkatasubbaiah, Krishnan

, p. 413 - 419 (2021/11/01)

One-pot synthesis of α-methyl ketones starting from 1,3-diaryl propenols or 1-aryl propenols and methanol as a C1 source is demonstrated. This one-pot isomerization-methylation is catalyzed by commercially available Pd(OAc)2 with H2O as the only by-product. Mechanistic studies and deuterium labelling experiments indicate the involvement of isomerization of allyl alcohol followed by methylation through a hydrogen-borrowing pathway in these isomerization-methylation reactions.

Long-Range Triplet Hydrogen Abstraction. Photochemical Formation of 2-Tetralols from β-Arylpropiophenones

Zhou, Boli,Wagner, Peter J.

, p. 6796 - 6799 (2007/10/02)

The four ketones β-(o-tolyl)- and β-mesitylpropiophenone and -isobutyrophenone all undergo photocyclization to 2-tetralols via triplet-state ε-hydrogen abstraction.The intermediate 1,6-biradicals cyclize in 100percent efficiency.The triplets react in very

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