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1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-5,6-dimethyl-2-phenyl- is a complex organic compound with the molecular formula C16H16N2O2. It is a derivative of isoindole, a heterocyclic aromatic compound containing a benzene ring fused to a pyrrolidine ring. The compound features a 1,3-dione group, which consists of two carbonyl groups (C=O) at the 1 and 3 positions, and a tetrahydro structure, indicating the presence of four hydrogen atoms in the molecule. Additionally, it has two methyl groups (-CH3) at the 5 and 6 positions, and a phenyl group (C6H5) attached to the 2 position. 1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-5,6-dimethyl-2-phenyl- is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various biologically active molecules.

96599-48-3

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96599-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96599-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,9 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96599-48:
(7*9)+(6*6)+(5*5)+(4*9)+(3*9)+(2*4)+(1*8)=203
203 % 10 = 3
So 96599-48-3 is a valid CAS Registry Number.

96599-48-3Downstream Products

96599-48-3Relevant academic research and scientific papers

Rate Enhancement in Ethanolic Aqueous Buffer. The Diels-Alder Reaction

Smith, Michael B.,Fay, Joseph N.,Son, Young Chan

, p. 2451 - 2454 (2007/10/02)

We have observed a 2.5 - 3-fold increase in the rate of Diels-Alder reactions when done in aqueous ethanol, where the aqueous solution was prepared with a pH 7 buffer.This is a simple, inexpensive and convenient method for modest acceleration of the Diels

5-ALKYLIDENE-HEXAHYDRO-1H-CYCLOPENTAPYRROL-1,3-DIONES BY NICKEL(0) OR PALLADIUM(0) CATALYZED CYCLOADDITION OF METHYLENECYCLOPROPANES WITH MALEIMIDES

Binger, Paul,Freund, Andreas,Wedemann, Petra

, p. 2887 - 2894 (2007/10/02)

Nickel(0) catalyzed cycloaddition of methylenecyclopropanes 1a-e with N-substituted maleimide 3b (R = CH3) and 3c (R = Ph) leads almost exclusively to the title compounds 6 and 7.The same reaction occurs in the presence of a palladium(0) catalyst wi

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