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2 bromo 1 phenyl ethanone

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2-bromo-1-phenyl ethanone is a chemical compound used as a laboratory reagent. It is a crystalline solid with a melting point of approximately 58-60°C. The compound is commonly used in organic synthesis and chemical research applications.

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Lab products found in correlation

Methanol, by Merck Group (1 mentions) Phenylhydrazine, by Merck Group (1 mentions) Dodecane, by Merck Group (1 mentions) Anisole, by Merck Group (1 mentions) Tempo, by Merck Group (1 mentions) Methanesulfonic acid, by Merck Group (1 mentions) Anthraquinone, by Merck Group (1 mentions) Benzoic anhydride, by Merck Group (1 mentions) Deuterated dimethyl sulfoxide dmso d6, by Merck Group (1 mentions) Sodium l ascorbate, by Merck Group (1 mentions) Sodium azide, by Merck Group (1 mentions) Deuterated methanol, by Merck Group (1 mentions) Deuterated chloroform, by Merck Group (1 mentions) Ethinyl estradiol, by Merck Group (1 mentions)

2 protocols using 2 bromo 1 phenyl ethanone

1

Synthesis of Substituted Phenyl Cyclohexenes

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Solvents (AR), including methanol, ethyl acetate, hexane, anisole, and dichloromethane (DCM), and the reagents, such as phenyl cyclohexene (>95%), anthraquinone, phenyl hydrazine, 2-bromo-1-phenyl ethanone, benzoic anhydride, BHT, TEMPO, methanesulfonic acid, and dodecane (>99%), were all purchased from Sigma-Aldrich. The reactant, 4-methoxy- substituted phenyl cyclohexene, in the reaction scope was prepared with the literature method, and other reactants were prepared with similar method (49 (link)).
Yang M., Lenarda A., Frindy S., Sang Y., Oksanen V., Bolognani A., Hendrickx L., Helaja J, & Li Y. (2023). A metal-free carbon catalyst for oxidative dehydrogenation of aryl cyclohexenes to produce biaryl compounds. Proceedings of the National Academy of Sciences of the United States of America, 120(31), e2303564120.
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2

Deuterated Solvents and Organohalogens Synthesis

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Deuterated chloroform (CDCl3, 99.8% with 0.5% tetramethylsilane-TMS), deuterated methanol (CD3OD, 99.9%), deuterated dimethylsulfoxide (DMSO-d6, 99.9%) and deuterated acetone (acetone-d6, 99.9%) were purchased from Sigma-Aldrich. Ethyl acetate and hexane were purchased from Synth. Sodium azide was purchased from Merck. The reagents 2-bromo-1-phenylethanone (98%), 2-bromo-1-(4-methoxyphenyl)ethanone (97%), 2-bromo-1-(4-chlorophenyl)ethanone (98%), 2-bromo-1-(4-bromophenyl)ethanone (98%), 2-bromo-1-(4-fluorinephenyl)ethanone (98%), 2-bromo-1-(3-fluorinephenyl)ethanone (98%), (+)-sodium L-ascorbate (98%) and ethinylestradiol (≥98%) were purchased from Sigma-Aldrich.
Queiroz T.M., Orozco E.V., Silva V.R., Santos L.S., Soares M.B., Bezerra D.P, & Porto A.L. (2019). Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, 5(9), e02408.
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