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Cis-4-benzyl-10-oxa-4-azatricyclo<5.2.1.0>decane-3,5-dione is a complex organic compound with the molecular formula C15H17NO3. It is a tricyclic molecule, featuring a benzyl group attached to the 4-position, an oxa bridge, and an aza group. The compound has two carbonyl groups at the 3 and 5 positions, which contribute to its reactivity and potential applications in various chemical reactions. This specific arrangement of atoms and functional groups gives it unique chemical properties, making it a valuable compound for research and development in the field of organic chemistry.

7802-31-5

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7802-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7802-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,8,0 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7802-31:
(6*7)+(5*8)+(4*0)+(3*2)+(2*3)+(1*1)=95
95 % 10 = 5
So 7802-31-5 is a valid CAS Registry Number.

7802-31-5Relevant academic research and scientific papers

Norcantharimides, synthesis and anticancer activity: Synthesis of new norcantharidin analogues and their anticancer evaluation

Hill, Timothy A.,Stewart, Scott G.,Ackland, Stephen P.,Gilbert, Jayne,Sauer, Benjamin,Sakoff, Jennette A.,McCluskey, Adam

, p. 6126 - 6134 (2008/03/27)

A range of amines was reacted with norcantharidin (2) to provide the corresponding norcantharimides (9-43). Treatment of norcantharidin with allylamine afforded the corresponding allyl-norcantharimide (20) which was amenable to epoxidation (mCPBA, 22) and

Oxazaborolidine catalysed enantioselective reduction of cyclic meso-imides

Ostendorf, Martin,Romagnoli, Romeo,Pereiro, Isabel Cabeza,Roos, Eric C.,Moolenaar, Marinus J.,Speckamp, W. Nico,Hiemstra, Henk

, p. 1773 - 1789 (2007/10/03)

Full details of the enantioselective reduction of cyclic meso-imides catalysed by an enantiopure oxazaborolidine derived from (S)-α,α-diphenylprolinol are reported. Treatment of the imides with borane in the presence of the catalyst led to a mixture of cis- and trans-hydroxylactams and, after subsequent ethanolysis, to the corresponding diastereomerically pure trans-ethoxylactams. The enantiomeric excesses were shown to be 68-94% by HPLC-determination. One example, in which the ethoxylactam was converted into the benzenesulfonyllactam, could be crystallized to >99% enantiomeric purity.

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