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ethyl 4-oxochromane-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153787-16-7

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153787-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153787-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,7,8 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153787-16:
(8*1)+(7*5)+(6*3)+(5*7)+(4*8)+(3*7)+(2*1)+(1*6)=157
157 % 10 = 7
So 153787-16-7 is a valid CAS Registry Number.

153787-16-7Relevant academic research and scientific papers

Highly Carbon-Selective Monofluoromethylation of β-Ketoesters with Fluoromethyl Iodide

Ding, Tianqi,Jiang, Lvqi,Yang, Jie,Xu, Yimin,Wang, Guixiang,Yi, Wenbin

supporting information, p. 6025 - 6028 (2019/08/20)

A highly carbon-selective monofluoromethylation of a broad range of β-ketoesters with fluoromethyl iodide under mild conditions is described. The uses of lithium tert-butoxide as the base and diglyme as the solvent made great contributions to the high C/O regioselectivity.

5-AMINO-4-CARBAMOYL-PYRAZOLE COMPOUNDS AS SELECTIVE AND IRREVERSIBLE T790M OVER WT-EGFR KINASE INHIBITORS AND USE THEREOF????

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Paragraph 0223, (2016/03/13)

Disclosed are compounds of Formula (I), pharmaceutical compositions comprising the same, processes for the preparation thereof, and the use thereof.

Regioswitchable Palladium-Catalyzed Decarboxylative Coupling of 1,3-Dicarbonyl Compounds

Kenny, Miles,Christensen, Jeppe,Coles, Simon J.,Franckeviius, Vilius

supporting information, p. 3926 - 3929 (2015/08/19)

A palladium-catalyzed chemo- and regioselective coupling of 1,3-dicarbonyl compounds via an allylic linker has been developed. This reaction, which displays broad substrate scope, forms two C-C bonds and installs two all-carbon quaternary centers. The regioselectivity of the reaction can be predictably controlled by utilizing an enol carbonate of one of the coupling partners.

Convenient synthesis of chromones and quinolinones

Hemavathi,Naveen,Lokanatha Rai

, p. 409 - 410 (2013/09/24)

A one pot synthesis of substituted chromones and quinolinones by condensing commercially available and cheaper molecules like salicylic acid and anthranilic acid respectively with alkenes / nitriles followed by insitu cyclization using ammonium acetate as base has been achieved.

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