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(4-Hydroxy-2-indolyl)-3-phenylacrylnitril, also known as 4-hydroxyindole-3-phenyl-2-cyanoacrylate, is a chemical compound with the molecular formula C17H12N2O2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a phenyl group attached to the 3-position of the indole ring. The molecule also contains a nitrile group (-CN) at the 2-position and a hydroxyl group (-OH) at the 4-position. (4-Hydroxy-2-indolyl)-3-phenylacrylnitril is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and functional groups.

97369-46-5

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97369-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97369-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,6 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97369-46:
(7*9)+(6*7)+(5*3)+(4*6)+(3*9)+(2*4)+(1*6)=185
185 % 10 = 5
So 97369-46-5 is a valid CAS Registry Number.

97369-46-5Downstream Products

97369-46-5Relevant academic research and scientific papers

Hetero-Cope Rearrangements, III. - Vinylindoles via Hetero-Cope Rearrangement

Blechert, Siegfried

, p. 673 - 682 (2007/10/02)

The reaction of N-phenylnitrones 1 with allenes 2 which are substituted with electron acceptor groups gives various products via addition and sigmatropic rearrangement depending on the specific acceptor group.In this manner one obtains 2-substituted indoles 8a, 8b, and 10 from propadienyl trichloromethyl sulfoxide.Using phenyl propadienyl sulfone a derivative 4a of tetrahydro-1-benzazepin-4-one is obtained.Reactions with allenecarbonitril proceed via several steps and yield 2-vinylindoles of type 6.Intermediate products could not be isolated.

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