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exo-3a,9a-dihydro-1,3-dioxo-2-phenyl-4,9-(toluene-p-sulphonyl)epiminobenzisoindoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86594-69-6

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86594-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86594-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,9 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86594-69:
(7*8)+(6*6)+(5*5)+(4*9)+(3*4)+(2*6)+(1*9)=186
186 % 10 = 6
So 86594-69-6 is a valid CAS Registry Number.

86594-69-6Downstream Products

86594-69-6Relevant academic research and scientific papers

Efficient synthesis of isoindoles using supercritical carbon dioxide

Ito, Satoshi,Akaki, Masayuki,Shinozaki, Yasutaka,Iwabe, Yuuki,Furuya, Masaru,Tobata, Marina,Roppongi, Makoto,Sato, Takafumi,Itoh, Naotsugu,Oba, Toru

, p. 1338 - 1342 (2017/03/10)

Bicyclopyrroles were efficiently converted to the corresponding isoindoles by a retro Diels-Alder reaction in supercritical carbon dioxide. By adding ethylene gas as an oxygen scavenger, the isoindole yield was further improved.

SUBSTITUTION AND ADDITION REACTIONS OF ISOINDOLES

Bonnett, Raymond,North, Stephanie A.,Newton, Roger F.,Scopes, David I. C.

, p. 1401 - 1406 (2007/10/02)

1-Phenylisoindole reacts with toluene-p-diazonium chloride to give the azo derivative formed by electrophilic substitution at the free α position.However, attempted nitrosation of 1-phenylisoindole gave the product (3) of oxidative dimerisation, while the

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