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5,11-Epoxy-5H-pyrido[3,4-b]carbazole, 10,11-dihydro-5,11-dimethyl-10-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92399-44-5

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92399-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92399-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,9 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92399-44:
(7*9)+(6*2)+(5*3)+(4*9)+(3*9)+(2*4)+(1*4)=165
165 % 10 = 5
So 92399-44-5 is a valid CAS Registry Number.

92399-44-5Relevant academic research and scientific papers

Synthesis and cytotoxicity of novel bisellipticines and bisisoellipticines

Obaza-Nutaitis, Judy A.,Gribble, Gordon W.

, p. 171 - 187 (2019/07/31)

A series of bis-ellipticines 7-9 and bis-isoellipticines 10-12 tethered through the indole nitrogen was synthesized and screened for antitumor cytotoxicity in the L-1210 murine leukemia assay. Activity was only displayed by 1,10-bis(6-ellipticinyl)-?-decane (8).

Synthesis and Diels-Alder Reactions of 1,3-Dimethyl-4-(phenylsulfonyl)-4H-furoindole. A new Annulation Strategy for the Construction of Ellipticine and Isoellipticine

Gribble, Gordon W.,Saulnier, Mark G.,Sibi, Mukund P.,Obaza-Nutaitis, Judy A.

, p. 4518 - 4523 (2007/10/02)

The novel fused heterocycle 1,3-dimethyl-4-(phenylsulfonyl)-4H-furoindole (4) is synthesized from 3-ethylindole (6) in six steps (46percent yield) or from indole-3-carboxaldehyde (12) in four steps (21percent yield).Furoindole 4 undergoes Diels-Alder reactions with dimethyl acetylenedicarboxylate, N-phenylmaleimide, benzyne, and 3,4-pyridyne (5) to give the expected adducts 17, 18a,b, 19, and 23a,b, respectively.Deoxygenation and desulfonylation of 19 and 23a,b, respectively, give benzocarbazole 22 and a readily separable mixture of the pyridocarbazole alkaloids ellipticine (1a) and isoellipticine (2a).

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