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2(3H)-Benzoxazolone, 5-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54209-92-6

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54209-92-6 Usage

Molecular Weight

163.13 g/mol

Chemical Family

Benzoxazolone

Derivative

Contains a hydroxy group at the 5th position

Usage

Building block in the synthesis of pharmaceuticals, agrochemicals, and organic materials

Biological Activities

Exhibits potential antioxidant and anti-inflammatory properties

Potential Applications

Treatment of neurodegenerative diseases, fluorescent probe in biochemical and biomedical research

Field of Use

Chemistry and medicine

Check Digit Verification of cas no

The CAS Registry Mumber 54209-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54209-92:
(7*5)+(6*4)+(5*2)+(4*0)+(3*9)+(2*9)+(1*2)=116
116 % 10 = 6
So 54209-92-6 is a valid CAS Registry Number.

54209-92-6Relevant academic research and scientific papers

TRIAZOLOPYRIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF

-

Page/Page column 328, (2015/03/28)

Compounds of Formula 0, Formula I and Formula II and methods of use as Janus kinase inhibitors are described herein.

Optimization of N-benzyl-benzoxazol-2-ones as receptor antagonists of macrophage migration inhibitory factor (MIF)

Hare, Alissa A.,Leng, Lin,Gandavadi, Sunilkumar,Du, Xin,Cournia, Zoe,Bucala, Richard,Jorgensen, William L.

scheme or table, p. 5811 - 5814 (2010/12/20)

The cytokine MIF is involved in inflammation and cell proliferation via pathways initiated by its binding to the transmembrane receptor CD74. MIF also exhibits keto-enol tautomerase activity, believed to be vestigial in mammals. Starting from a 1 μM hit from virtual screening, substituted benzoxazol-2-ones have been discovered as antagonists with IC50 values as low as 7.5 nM in a tautomerase assay and 80 nM in a MIF-CD74 binding assay. Additional studies for one of the potent inhibitors demonstrated that it is not a covalent inhibitor of MIF and that it attenuates MIF-dependent ERK1/2 phosphorylation in human synovial fibroblasts.

Fast deprotection of phenoxy benzyl ethers in transfer hydrogenation assisted by microwave

Quai, Monica,Repetto, Claudio,Barbaglia, Walter,Cereda, Enzo

, p. 1241 - 1245 (2007/10/03)

Phenoxy benzyl ethers are easily and quickly deprotected in the presence of ammonium formate and microencapsulated Pd(0)EnCat with the assistance of microwave irradiation. This procedure can be applied in the presence of other functional groups as well. The described protocol is particularly convenient for the preparation in a parallel and automatic fashion of libraries of compounds possessing a phenol type moiety.

Glucosides from MBOA and BOA detoxification by Zea mays and Portulaca oleracea

Hofmann, Diana,Knop, Mona,Hao, Huang,Hennig, Lothar,Sicker, Dieter,Schulz, Margot

, p. 34 - 37 (2008/09/21)

Incubation of Zea mays cv. Nicco seedlings with 6-methoxybenzoxazolin-2(3#) -one (MBOA) led to a minor detoxification product hitherto only found in Poaceae. This new compound was identified as 1-(2-hydroxy-4-methoxyphenylamino)- 1-deoxy-β-glucoside 1,2-c

NOVEL HETEROCYCLIC COMPOUND

-

Page/Page column 72, (2010/11/24)

A drug having a high affinity for benzodiazepine ω3 receptors and showing curative and preventive effects for anxiety and depression, which comprises as the active ingredient, for example, a compound of the formula (1): wherein R1 an

Introduction of a hydroxy group at the para position and N-iodophenylation of N-arylamides using phenyliodine(III) bis(trifluoroacetate)

Itoh, Naoki,Sakamoto, Takeshi,Miyazawa, Etsuko,Kikugawa, Yasuo

, p. 7424 - 7428 (2007/10/03)

The reaction of anilides with phenyliodine(III) bis(trifluoroacetate) (PIFA) in trifluoroacetic acid (TFA), TFA-CHCl3, or hexafluoroisopropyl alcohol (HFIP) is described. When the acyl group of the anilide is highly electronegative, such as trifluoroacetyl, or the phenyl group is substituted with an electron-withdrawing group, the 4-iodophenyl group is transferred from PIFA to the amide nitrogen to afford acetyldiarylamines. On the other hand, when the acyl group contains an electron-donating function, such as 4-methoxyphenyl, or the phenyl group is substituted with an electron-donating group, a trifluoroacetoxy group is transferred to the para position of the anilide aromatic ring. This group is hydrolyzed during workup to produce the corresponding phenol.

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