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(E)-1-acetyl-2-benzylideneindolin-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132114-99-9

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132114-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132114-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132114-99:
(8*1)+(7*3)+(6*2)+(5*1)+(4*1)+(3*4)+(2*9)+(1*9)=89
89 % 10 = 9
So 132114-99-9 is a valid CAS Registry Number.

132114-99-9Relevant academic research and scientific papers

A new palladium-catalyzed synthesis of indoxyl derivatives

An, Zhong-wei,Catellani, Marta,Chiusoli, Gian Paolo

, p. C31 - C32 (1990)

The reaction of iodoanilines with phenylacetylene and carbon monoxide catalyzed by a palladium(0) catalyst leads to indoxyl derivatives.

AURONES AND METHODS OF USING AURONES TO TREAT TUBERCULOSIS

-

Page/Page column 28, (2020/11/12)

This disclosure describes compounds, compositions, and methods for treating or preventing infection or disease including, in some specific embodiments, treating or preventing tuberculosis and/or infection with Mycobacterium tuberculosis (Mtb). In one aspect, this disclosure describes aurones including, for example, aurone 9504, aurone 9505, aurone 9501, aurone 9510, aurone AA2A, and aurone AA8, compositions including aurones, and methods of using aurones for treating or preventing tuberculosis.

N-heterocyclic carbene catalyzed formal [3+2] annulation reaction of enals: An efficient enantioselective access to spiro-heterocycles

Guo, Chang,Schedler, Michael,Daniliuc, Constantin G.,Glorius, Frank

supporting information, p. 10232 - 10236 (2015/03/31)

A highly enantioselective N-heterocyclic carbene (NHC) catalyzed formal [3+2] annulation of α,β-unsaturated aldehydes with azaaurones or aurone generating spiro-heterocycles has been developed. The protocol represents a unique NHC-activation-based approach to access spiro-heterocyclic derivatives bearing a quaternary stereogenic center with high optical purity (up to 95 % ee).

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