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8-benzyl-6-ethoxycarbonyl-1-hydroxy-4,4-diphenyl-8-aza-2,3-dioxabicyclo<4.3.0>nonan-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188741-87-9

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188741-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188741-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,4 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 188741-87:
(8*1)+(7*8)+(6*8)+(5*7)+(4*4)+(3*1)+(2*8)+(1*7)=189
189 % 10 = 9
So 188741-87-9 is a valid CAS Registry Number.

188741-87-9Relevant academic research and scientific papers

Palladium-catalyzed hydrogenolysis of azabicyclic peroxides. Quantitative transformation to 1-hydroxy-7-aza-2-oxabicyclo[3.3.0]octanes

Chowdhury, Firoz Alam,Kajikawa, Shougo,Nishino, Hiroshi,Kurosawa, Kazu

, p. 3765 - 3768 (2007/10/03)

The palladium-catalyzed reduction of 1-hydroxy-8-aza-2,3- dioxabicyclo[4.3.0]nonanes, which were readily obtained by the manganese(III)-mediated oxidative formal [2+2+2] cycloaddition of pyrrolidinedione derivatives with alkenes and molecular oxygen, led

Mn(III)-based reaction of alkenes with pyrrolidinedione derivatives. Formation of bicyclic peroxides and the related compounds

Nguyen, Van-Ha,Nishino, Hiroshi,Kurosawa, Kazu

, p. 465 - 480 (2007/10/03)

Alkenes (1) and 2,3-pyrrolidinediones (2) were treated with manganese(III) acetate in acetic acid at 23°C under a stream of dry air giving 1-hydroxy-8-aza-2,3-dioxabicyclo[4.3.0]nonan-9-ones (3) in good yields. The reaction at elevated temperature gave 4-ethenyl-2,3-pyrrolidinediones (6) and/or 4-alkyl-2,3-pyrrolidinediones (7) in good yields. A wide variety of 2,3-pyrrolidinediones having an alkoxycarbonyl, cyano, or acyl group at the 4-position were tested to delineate the scope and limitations of these reactions. The mechanisms for the formation of the products were also discussed.

Mn(III)-Induced molecular oxygen trapping reaction of alkenes with 2,3-pyrrolidinedione derivatives. A novel entry to 1-hydroxy-8-aza-2,3-dioxabicyclo[4.3.0]nonan-9-ones

Nguyen, Van-Ha,Nishino, Hiroshi,Kurosawa, Kazu

, p. 1773 - 1776 (2007/10/03)

Molecular oxygen trapping reaction of alkenes with 2,3-pyrrolidinedione derivatives was developed using a Mn(III)-induced oxidation system. Alkenes and 2,3-pyrrolidinediones were treated with manganese(III) acetate in acetic acid under a stream of dry air, giving 1-hydroxy-8-aza-2,3-dioxabicyclo[4.3.0]nonan-9-ones in good yields, The reaction involved molecular oxygen trapping of radicals which were formed by the addition of pyrrolidinedione radicals induced by Mn(III) to alkenes.

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