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(2R,3R)-2-Ethyl-2-phenyl-2,3-dihydro-1H-indol-3-ol is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of compounds known as indoles. This specific compound features a 2,3-dihydro-1H-indol-3-ol core, which is a reduced form of the indole ring system, with an ethyl group at the 2-position and a phenyl group at the 3-position. The (2R,3R) configuration indicates that both the 2-ethyl and 3-phenyl substituents are in the R configuration, which affects the compound's stereochemistry and potential biological activity. (2R,3R)-2-Ethyl-2-phenyl-2,3-dihydro-1H-indol-3-ol may be of interest in the fields of organic chemistry and medicinal chemistry due to its structural features and potential applications in the synthesis of pharmaceuticals or other bioactive molecules.

66152-10-1

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66152-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66152-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66152-10:
(7*6)+(6*6)+(5*1)+(4*5)+(3*2)+(2*1)+(1*0)=111
111 % 10 = 1
So 66152-10-1 is a valid CAS Registry Number.

66152-10-1Relevant academic research and scientific papers

Stereoselective Reduction of Indoline Nitroxide Radicals

Berti, Corrado,Greci, Lucedio,Poloni, Marino

, p. 710 - 713 (2007/10/02)

1,2-Dihydro-2-alkyl-2-phenyl-3H-indol-3-one 1-oxyls (1) and the corresponding amines (6) undergo stereoselective reduction with NaBH4 giving respectively a pair of diastereoisomeric hydroxylamines (2), (3) and the corresponding amines (7), (8).Both lead to nitroxide radicals (4) and (5), by oxidation; the quantitative ratio of diastereoisomers was determined by liquid-liquid chromatography.The configurations of the isomers are tentatively assigned on the basis of (1)H n.m.r. and e.s.r. data, as well as on the stereochemistry of the reaction.

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