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6,6-dimethyl-1-phenyl-6,7-dihydro-1H-indazol-4(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

43102-70-1

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43102-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43102-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,0 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 43102-70:
(7*4)+(6*3)+(5*1)+(4*0)+(3*2)+(2*7)+(1*0)=71
71 % 10 = 1
So 43102-70-1 is a valid CAS Registry Number.

43102-70-1Relevant academic research and scientific papers

Ultrasound assisted regioselective synthesis, photophysical and structural studies of 1-substituted indazol-4(5H)-ones and enaminodiketones of dimedone

Chaudhary, R. P.,Gautam, Deepika,Gautam, Poonam,Mittal, Isha

, (2020/12/23)

Enaminodiketone, obtained from reaction of dimedone with DMF-DMA, on reaction with nucleophiles such as amines, guanidine hydrochloride and substituted aromatic hydrazines furnished enaminodiketones, quinazolines and indazole derivatives respectively. The

Carbodiimide mediated synthesis of new thiazolidin-4-ones and thiazinan-4-ones from thiosemicarbazone derivatives of 6,7-dihydro-1H-indazole- 4(5H )-ones

Gautam, Poonam,Chaudhary, Ram P.

, p. 226 - 230 (2014/05/06)

5,5-Dimethyl-2-[(2-substitutedphenylhydrazinyl)methylene]cyclohexane-1, 3-dione, obtained from heating dimedone with N,N'-dimethylformamide dimethyl acetal (DMF-DMA) and phenyl hydrazines, on cyclisation in ethanol gave 6,7-dihydro- 1H-indazol-4(5H )-ones

Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. I. Synthesis of 1,5-Disubstituted 4-Acylpyrazoles

Schenone, Pietro,Mosti, Luisa,Menozzi, Giulia

, p. 1355 - 1361 (2007/10/02)

Reaction of open-chain and cyclic sym-1,3-diones with N,N-dimethylformamide dimethyl acetal gave, generally in high yield, a series of sym-2-dimethylaminomethylene-1,3-diones which reacted with phenylhydrazine and methylhydrazine to afford, generally in satisfactory yield, a number of 1,5-disubstituted 4-acylpyrazoles.The applications and limits of this new pyrazole synthesis are presented and discussed.

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