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Methanone, (2,5-dimethylphenyl)(2-fluorophenyl)-, also known as 1-(2,5-dimethylphenyl)-2-(2-fluorophenyl)ethanone, is an organic compound with the molecular formula C15H13FO. It is a derivative of acetophenone, featuring a fluorine atom in the ortho position of the phenyl ring and two methyl groups in the para position of the other phenyl ring. This chemical is characterized by its unique structure, which may influence its reactivity and physical properties. It is typically used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its potential to form different types of chemical bonds and its ability to act as a building block in more complex molecular structures.

2250-60-4

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2250-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2250-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2250-60:
(6*2)+(5*2)+(4*5)+(3*0)+(2*6)+(1*0)=54
54 % 10 = 4
So 2250-60-4 is a valid CAS Registry Number.

2250-60-4Downstream Products

2250-60-4Relevant academic research and scientific papers

Controlled photo-flow oxidative reaction (UV-FOR) platform for ultra-fast phthalide and API synthesis

Aand, Dnyaneshwar,Karekar, Sanjeev,Mahajan, Bhushan,Pawar, Amit B.,Singh, Ajay K.

, p. 4584 - 4590 (2018/10/23)

An integrated photo-flow oxidative reaction (UV-FOR) platform approach is presented for the synthesis of phthalides. The current protocol is catalyst-free, and uses economical and abundant hydro-carbons and hydrocarbon derivatives such as benzoic acid, benzene, and xylene, as starting materials. The reaction is performed using oxygen as a green oxidant in a time- and labour-efficient manner. This integrated approach has been shown to be successful in making a UV-FOR platform suitable for the on-demand synthesis of phthalides and their further syntheses to 2-arylmethylbenzoic acids and arylogous Michael addition products under relatively mild conditions. The current protocol was further extended to the gram scale synthesis of an ischemic stroke-relevant active pharmaceutical ingredient (API), 3-N-butylphthalide (NBP), in a continuous flow process.

Friedel-Crafts acylation reaction using carboxylic acids as acylating agents

Kawamura, Masato,Cui, Dong-Mei,Shimada, Shigeru

, p. 9201 - 9209 (2007/10/03)

Dehydrative Friedel-Crafts acylation reaction of aromatic compounds with carboxylic acids as acylating agents was investigated in the presence of Lewis acid- or Br?nsted acid-catalyst. Various metal triflates and bis(trifluoromethanesulfonyl)amides showed catalytic activity at high temperature, among which Eu(NTf2)3 proved to be the most effective and efficiently catalyzed the acylation reaction of alkyl- and alkoxybenzenes with aliphatic and aromatic carboxylic acids at 250 °C. Bi(NTf2)3 was more effective than Eu(NTf2)3 at lower temperature, but proved to be hydrolyzed in the presence of a small amount of water to give HNTf2 and [Bi6O4(OH)4(H2O)6](NTf2)6. The structure of the latter compound was confirmed by a single crystal X-ray analysis. Among five Br?nsted acids, HOTf, HNTf2, HCTf3, TsOH, and Nafion SAC-13, HNTf2 has proved to be the most efficient catalyst and more effective than Eu(NTf2)3 for the acylation of p-xylene with heptanoic acid at 220 °C or lower temperature. HNTf2 catalyzed the acylation of anisole with carboxylic acids in high yields in refluxing toluene with azeotropic removal of water.

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