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(2R,3R)-2-Methyl-2-phenyl-2,3-dihydro-1H-indol-3-ol is a complex organic compound with a molecular formula of C16H17NO. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the specific configuration is indicated by the (2R,3R) notation. (2R,3R)-2-Methyl-2-phenyl-2,3-dihydro-1H-indol-3-ol features a 2,3-dihydro-1H-indol-3-ol core, which is a type of indole derivative, a class of heterocyclic compounds with a benzene ring fused to a pyrrole ring. The molecule has a methyl group at the 2-position and a phenyl group at the same position, indicating a substitution pattern that affects its physical and chemical properties. It is an important intermediate in the synthesis of various pharmaceuticals and is known for its potential biological activities. The compound's structure and stereochemistry play a crucial role in determining its reactivity and potential applications in the field of drug development.

66152-09-8

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66152-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66152-09-8 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, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66152-09:
(7*6)+(6*6)+(5*1)+(4*5)+(3*2)+(2*0)+(1*9)=118
118 % 10 = 8
So 66152-09-8 is a valid CAS Registry Number.

66152-09-8Relevant 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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