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2H-Indol-2-one, 3-[(dimethylamino)methylene]-1-ethyl-1,3-dihydro-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141210-65-3

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141210-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141210-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141210-65:
(8*1)+(7*4)+(6*1)+(5*2)+(4*1)+(3*0)+(2*6)+(1*5)=73
73 % 10 = 3
So 141210-65-3 is a valid CAS Registry Number.

141210-65-3Downstream Products

141210-65-3Relevant academic research and scientific papers

LACTAM AND AMIDE ACETALS. 69. SYNTHESIS AND PROPERTIES OF 3-(AMINOMETHYLENE)-2-INDOLINONE DERIVATIVES

Golovko, T. V.,Solov'eva, N. P.,Bogdanova, G. A.,Sheinker, Yu. N.,Granik, V. G.

, p. 952 - 959 (2007/10/02)

Oxindole derivatives reacted with the diethyl acetals of dimethylformamide and dimethylacetamide to give the corresponding derivatives of 3-(aminomethylene)-, (aminoethylidene)-, and (ethoxyethylidene)-2-indolinone.These products were then easily converted to N-aryl- and N-alkylaminomethyleneoxindoles upon treatment with aryl or alkyl amines.The alkylation of N,N-dimethylaminomethylene-2-indolinones by dimethyl sulfate and triethyloxonium tetrafluoroborate, and the reactions of the resulting methyl sulfates and tetrafluoroborates with nucleophilic reagents were studied.The configuration of the 3-(aminomethylene)-2-indolinone derivatives prepared at the enamine C=C double bond was investigated by NMR.The free energies of activation for the cis-trans isomerization were determined in a number of cases.

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