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1-Oxa-4-azaspiro[4.5]decan-7-one, 2,2,9,9-tetramethyl-4-(phenylmethyl)-3-thioxo is a complex organic compound with a unique molecular structure. It is characterized by a spiro ring system, which consists of a seven-membered azaspiro ring fused to a five-membered oxaspiro ring. The compound features a ketone group at the 7-position, a thioketal group at the 3-position, and a benzyl group attached to the 4-position. Additionally, it has two methyl groups at the 2-position and two methyl groups at the 9-position, contributing to its overall stability and reactivity. 1-Oxa-4-azaspiro[4.5]decan-7-one, 2,2,9,9-tetramethyl-4-(phenylmethyl)-3-thioxo- is of interest in the field of organic chemistry, potentially for its applications in pharmaceuticals or as a synthetic intermediate.

91306-27-3

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91306-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91306-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,0 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91306-27:
(7*9)+(6*1)+(5*3)+(4*0)+(3*6)+(2*2)+(1*7)=113
113 % 10 = 3
So 91306-27-3 is a valid CAS Registry Number.

91306-27-3Downstream Products

91306-27-3Relevant academic research and scientific papers

Base-promoted Reactions of β-Enaminones with 2-Bromo-2-methylpropanamides. Formation of 2-Ketonyloxazolidin-4-ones and Cyclohexanespiro-oxazolidin-4-ones

Veronese, Augusto C.,Scrimin, Paolo,Vecchiati, Giorgio,Sferra, Stella,D'Angeli, Ferruccio

, p. 781 - 784 (2007/10/02)

Representative β-enaminones (1) and (2) react with N-alkyl-2-bromo-2-methylpropanamides (4a), (4b), and (4c) in the presence of NaH, to afford oxazolidin-4-ones (5) and (6) or spiro-oxazolidinone derivatives (7) and (8).The formation of an imidazolidin-4-one derivative (9) from 2-bromo-2-methylpropanilide (4c) is ascribed to the presence of an intermediate α-lactam (15).The behaviour of a spiro-oxazolidinone derivative on hydrolysis, reduction, and thiation is described.

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