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1-(4-methoxybenzoyl)-1,2-dihydro-3H-1,2-diazepin-3-one is a chemical compound with the molecular formula C16H16N2O3. It is a diazepinone derivative and belongs to the class of benzoyl compounds. 1-(4-methoxybenzoyl)-1,2-dihydro-3H-1,2-diazepin-3-one is characterized by its unique structure and properties, which make it a subject of interest in pharmaceutical research.

75267-93-5

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75267-93-5 Usage

Uses

Used in Pharmaceutical Research:
1-(4-methoxybenzoyl)-1,2-dihydro-3H-1,2-diazepin-3-one is used as a research compound for exploring its biological activity and potential therapeutic effects. Its structure and properties suggest that it may have applications in the development of new drugs, particularly in the pharmaceutical industry.
Further research is necessary to fully understand the potential uses and effects of 1-(4-methoxybenzoyl)-1,2-dihydro-3H-1,2-diazepin-3-one, as its current applications are primarily limited to the realm of pharmaceutical research and development. As our understanding of 1-(4-methoxybenzoyl)-1,2-dihydro-3H-1,2-diazepin-3-one grows, it may eventually find its way into various applications across different industries, similar to how gallotannin has been utilized in anticancer applications and drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 75267-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75267-93:
(7*7)+(6*5)+(5*2)+(4*6)+(3*7)+(2*9)+(1*3)=155
155 % 10 = 5
So 75267-93-5 is a valid CAS Registry Number.

75267-93-5Downstream Products

75267-93-5Relevant academic research and scientific papers

Photochemical Syntheses of 1,2-Diazepines. 11. Regiospecific Synthesis of 1,2-Dihydro-1,2-diazepin-3-ones

Kiguchi, Toshiko,Schuppiser, Jean-Luc,Schwaller, Jean-Claude,Streith, Jacques

, p. 5095 - 5100 (2007/10/02)

Starting from 2-chloropyridine 7, a series of 1,2-diazepin-3-ones 16 was prepared by a five-step synthesis.The key intermediates were the bicyclic oxadiazolium salts 10 which led, through a methoxide ion induced ring opening, to the expected 2-methoxypyri

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