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6-(bromomethyl)-4-(3-methoxypropyl)-2H-benzo[b][1,4]oxazin-3(4H)-one is a benzooxazinone derivative with the molecular formula C15H18BrNO3. It features a benzene ring fused to an oxazinone ring, along with a bromomethyl group and a 3-methoxypropyl group. This unique structural composition endows the compound with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, and suggests its possible biological activity or candidacy as a drug.

911705-42-5

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911705-42-5 Usage

Uses

Used in Pharmaceutical Industry:
6-(bromomethyl)-4-(3-methoxypropyl)-2H-benzo[b][1,4]oxazin-3(4H)-one is used as a potential drug candidate for its unique structural properties that may contribute to biological activity. Further research is required to explore its therapeutic potential and efficacy in treating specific medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 6-(bromomethyl)-4-(3-methoxypropyl)-2H-benzo[b][1,4]oxazin-3(4H)-one may be utilized as a component in the development of new pesticides or herbicides, leveraging its chemical structure to target and control pests or weeds effectively.
Used in Materials Science:
6-(bromomethyl)-4-(3-methoxypropyl)-2H-benzo[b][1,4]oxazin-3(4H)-one is used in materials science for its potential to contribute to the development of novel materials with specific properties, such as improved stability, reactivity, or other characteristics that can be beneficial in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 911705-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,7,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 911705-42:
(8*9)+(7*1)+(6*1)+(5*7)+(4*0)+(3*5)+(2*4)+(1*2)=145
145 % 10 = 5
So 911705-42-5 is a valid CAS Registry Number.

911705-42-5Relevant academic research and scientific papers

Substituted piperidines as inhibitors of beta-secretase, cathepsin D, plasmepsin II and/or HIV protease

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Page/Page column 61, (2008/12/07)

Use of compounds of the general formula (I) or (II) and pharmaceutically acceptable salt thereof, in which R, R1, R2, R3, R4, Q, W, X and Z, n and m have the definitions illustrated in detail in the description,

Organic compounds

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Page/Page column 48, (2010/11/30)

The present invention relates to substituted piperidines of the general formula (I), where R1, R2, R3, R4, R5, Q and X have the definitions elucidated in more detail in the description, to a process for their preparation and to the use of these compounds as medicines, in particular as renin inhibitors. Moreover, the enzymatic substrate portion of the compound is simultaneously a substrate for a membrane transporter.

SUBSTITUTED PIPERIDINES

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Page/Page column 41; 81, (2010/11/24)

SP-P2140 ATE - 132 - Abstract Novel substituted piperidines of the general formula (I) and (II) with the substituent definitions as explained in detail in the description are described. The compounds are suitable in particular as renin inhibitors and are

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