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4H-1-Benzopyran-4-one, 2-benzoyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51685-51-9

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51685-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51685-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,8 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51685-51:
(7*5)+(6*1)+(5*6)+(4*8)+(3*5)+(2*5)+(1*1)=129
129 % 10 = 9
So 51685-51-9 is a valid CAS Registry Number.

51685-51-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzoylchromen-4-one

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-one,2-benzoyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51685-51-9 SDS

51685-51-9Relevant academic research and scientific papers

Lewis acid-triggered selective zincation of chromones, quinolones, and thiochromones: Application to the preparation of natural flavones and isoflavones

Klier, Lydia,Bresser, Tomke,Nigst, Tobias A.,Karaghiosoff, Konstantin,Knochel, Paul

supporting information; experimental part, p. 13584 - 13587 (2012/10/08)

A Lewis acid-triggered zincation allows the regioselective metalation of various chromones and quinolones. In the absence of MgCl2, a C(3) zincation is observed, whereas in the presence of MgCl2 or a related Lewis acid, C(2) zincation occurs. Applications to a natural flavone, isoflavone, and quinolone are shown.

2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ) mediated oxidationdehydrogenation of 2-aroyl-3,4-dihydro-2H-benzopyrans : Synthesis of 2-aroylbenzopyran-4-ones

Chen, Liang-Yeu,Li, Sie-Rong,Chen, Po-Yuan,Chang, Ho-Chiang,Wang, Tzu-Pin,Wang, Eng-Chi,Tsai, Ian-Lih

experimental part, p. 64 - 76 (2010/12/19)

DDQ mediated an oxidation-dehydrogenation of 2-aroyl-3,4-dihydro-2H- benzopyran prepared from salicylaldehyde to yield 2-aroylbenzopyran-4-one. Stochiometric amount of DDQ, acetic acid and water in refluxing dioxane are the optimal condition for this oxidation-dehydrogenation reaction. A rationally proposed mechanism for this oxidation-dehydrogenation process is based on the isolation of a reaction intermediate viz., 2-benzoyl-8-methoxy-3,4- dihydrobenzopyran-4-one and the identification of the 18O-labled carbonyl group of benzopyran-4-one demonstrating incorporation of labeled H 218O.

Benzenesulfonylimine derivatives as inhibitors of IL-1 action

-

, (2008/06/13)

The present invention relates to novel benzenesulfonylimine derivatives and their use as inhibitors of Interleukin-1 (IL-1) action. Such inhibitors are useful in the treatment of various disease states as disclosed herein including: rheumatoid arthritis,

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