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1-(3-fluoro-benzyl)-1H-benzo[d][1,3]oxazine-2,4-dione is a complex organic compound with a molecular formula of C15H10FNO3. It features a benzene ring with a fluorine atom at the 3-position, attached to a benzoxazine-2,4-dione core. The benzoxazine-2,4-dione moiety consists of a benzene ring fused to an oxazine ring, with two carbonyl groups at the 2 and 4 positions. 1-(3-fluoro-benzyl)-1H-benzo[d][1,3]oxazine-2,4-dione is characterized by its unique structure, which may exhibit specific chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. However, further research and characterization are needed to fully understand its properties and potential uses.

57384-89-1

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57384-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57384-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,8 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57384-89:
(7*5)+(6*7)+(5*3)+(4*8)+(3*4)+(2*8)+(1*9)=161
161 % 10 = 1
So 57384-89-1 is a valid CAS Registry Number.

57384-89-1Downstream Products

57384-89-1Relevant academic research and scientific papers

Synthesis and antibiofilm evaluation of 3-hydroxy-2,3-dihydroquinazolin-4(1H)-one derivatives against opportunistic pathogen Acinetobacter baumannii

Yang, Guo,Cheng, Cheng,Xu, Guo-Bo,Tang, Lei,Chua, Kim-Lee,Yang, Yuan-Yong

, (2020/07/07)

The emergence of multidrug resistant microorganisms has triggered the impending need for new aitimicrobial strategies. The antivirulence strategy with the benefite of alleviating the drug resistance becomes the focus of research. In this study, 22 quorum sensing inhibitors were synthesized by mimicking the structure of autoinducer and acinetobactin and up to 34% biofilm inhibition was observed with 5u. The biofilm inhibition effect was further demonstrated with extracellular polysaccharides inhibition and synergism with Gentamycin sulphate.

The chemistry of 2H-3,1-benzoxazine-2,4(1H)-dione (isatoic anhydride). XXIV. N-benzylation of isatoic anhydride under mitsunobu conditions

Coppola, Gary M.

, p. 1009 - 1013 (2007/10/03)

Isatoic anhydride is readily alkylated on nitrogen with benzylic alcohols in the presence of triphenylphosphine and diethyl azodicarboxylate. Both electron donating and electron withdrawing groups are tolerated.

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