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(6,11-dihydro-6,11-dioxonaphth<2,3-b>indolizin-12-yl)carbonylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33879-91-3

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33879-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33879-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,8,7 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33879-91:
(7*3)+(6*3)+(5*8)+(4*7)+(3*9)+(2*9)+(1*1)=153
153 % 10 = 3
So 33879-91-3 is a valid CAS Registry Number.

33879-91-3Relevant academic research and scientific papers

Synthesis, Characterization and Photophysical Properties of Naphtho[2,3-b]Indolizine-6,11-Dione Derivatives

Batenko, Nelli,Neibolte, Ilze,Belyakov, Sergey,Valters, Raimonds

, p. 23 - 29 (2016)

This communication concerns the synthesis, structural characterization and fluorescent properties of novel naphtho[2,3-b]indolizine-6,11-dione derivatives. The target compound synthesized by one-pot multicomponent reaction between naphthoquinone, indandio

Reaction of Monothio-derivatives of 2-Heteroarylideneindene-1,3(2H)-diones with Quinones

Buggle, Katherine,Power, Joseph

, p. 1070 - 1075 (2007/10/02)

The reaction of 2,3-dihydro-2--3-thioxoinden-1-one (5) with 1,4-benzoquinone and with 1,4-naphthoquinone in alcohols afforded thiobenzoylindolizinoquinones (7) and (12) which were characterised by spectroscopy and by oxidation and redu

Heterocyclic Quinonoid Chromophoric Systems: Part VI- Reaction of 2,3-Dichloro-1,4-naphthoquinone with Homophthalimides Other Compounds Containing a Reactive Methylene Group

Ayyangar, N. R.,Kolhe, P. Y.,Tilak, B. D.

, p. 836 - 843 (2007/10/02)

Interaction of 2,3-dichloro-1,4-naphthoquinone (1) with homophthalimides (2a-2c) and other open chain and cyclic compounds containing a reactive methylene group in presence of pyridine is described.The reaction affords 12-substituted naphthindolizinediones (4,5).A plausible reaction mechanism for the formation of the latter compounds is discussed.

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