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Methanone, (2,5-dimethylphenyl)(4-fluorophenyl)-, also known as 1-(2,5-dimethylphenyl)-4-fluorobenzene, is an organic compound with the chemical formula C14H13FO. It is a derivative of acetophenone, featuring a fluorine atom attached to a phenyl ring, which distinguishes it from other acetophenone derivatives. Methanone, (2,5-dimethylphenyl)(4-fluorophenyl)- is characterized by its molecular structure, which includes two phenyl rings connected by a carbonyl group, with one phenyl ring bearing two methyl groups at the 2nd and 5th positions, and the other phenyl ring having a fluorine atom at the 4th position. Methanone, (2,5-dimethylphenyl)(4-fluorophenyl)-, is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties.

2250-61-5

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2250-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2250-61-5 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 2250-61:
(6*2)+(5*2)+(4*5)+(3*0)+(2*6)+(1*1)=55
55 % 10 = 5
So 2250-61-5 is a valid CAS Registry Number.

2250-61-5Downstream Products

2250-61-5Relevant 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.

supporting information, 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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