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2-(4-aminophenyl)-3a,5-dimethyl-3a,4,7,7a-tetrahydro-3H-pseudoindol-4-one is a complex organic compound with a molecular formula of C16H18N2O. It is a derivative of pseudoindolone, a heterocyclic compound with a structure similar to indole but with a carbonyl group replacing one of the carbon atoms in the ring. This specific compound features a 4-aminophenyl group attached to the 2-position of the pseudoindolone core, which contributes to its unique chemical properties. The presence of two methyl groups at the 3a and 5 positions, along with the tetrahydro structure, further distinguishes it from other pseudoindolone derivatives. 2-(4-aminophenyl)-3a,5-dimethyl-3a,4,7,7a-tetrahydro-3H-pseudoindol-4-one may have potential applications in pharmaceuticals or as a building block in the synthesis of more complex molecules, but its specific uses and properties would require further investigation and characterization.

75601-05-7

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75601-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75601-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,0 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75601-05:
(7*7)+(6*5)+(5*6)+(4*0)+(3*1)+(2*0)+(1*5)=117
117 % 10 = 7
So 75601-05-7 is a valid CAS Registry Number.

75601-05-7Downstream Products

75601-05-7Relevant academic research and scientific papers

Rearrangement of arylhydrazones of aromatic and arylaliphatic carbonyl compounds to biphenyl derivatives. 3

Fusco, R.,Sannicolo, F.

, p. 83 - 89 (2007/10/02)

The behavior toward polyphosphoric acid of arylhydrazones of aromatic carbonyl compounds (anisaldehyde, substituted benzophenones, (4-methoxyphenyl)glyoxylic acid esters) and arylaliphatic ketones (4-methoxy- and 4-aminoacetophenone) is described.Biphenyl derivatives are formed through a sigmatropic rearrangement, which often occurs in competition with the expected Fischer indole synthesis and, in the case of the 4-amino-acetophenone 2,6-dimethylphenylhydrazone, with a completely new sigmatropic rearrangement.

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