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3-Ethylindolo[2,3-a]quinolizine is a complex organic compound with the molecular formula C14H14N2. It belongs to the class of indoloquinolizine alkaloids, which are naturally occurring heterocyclic compounds found in various plants. This specific compound is characterized by its unique structure, featuring an indoloquinolizine core with an ethyl group attached to the 3-position. It is known for its potential biological activities and has been studied for its possible applications in pharmaceutical research. The compound's properties, such as solubility and stability, can be influenced by its molecular structure and the presence of functional groups. While the specific applications and effects of 3-ethylindolo[2,3-a]quinolizine are not detailed here, it is an area of interest for scientists exploring the therapeutic potential of natural products.

486-18-0

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486-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 486-18-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 486-18:
(5*4)+(4*8)+(3*6)+(2*1)+(1*8)=80
80 % 10 = 0
So 486-18-0 is a valid CAS Registry Number.

486-18-0Downstream Products

486-18-0Relevant academic research and scientific papers

Short synthetic route to 5,6-dihydroflavopereirine and flavopereirine

Lounasmaa, Mauri,Hanhinen, Pirjo,Lipponen, Sami

, p. 1365 - 1370 (2007/10/03)

A short synthetic route to 5,6-dihydroflavopereirine (1) and flavopereirine (2) is described.

Syntheses of Camalexin, Indolopyridocoline and Flavopereirine

Fuerstner, Alois,Ernst, Andreas

, p. 773 - 786 (2007/10/02)

A short synthetic route to the phytoalexin camalexin 7 and a convergent approach to the alkaloids indolopyridocoline 8, 6,7-dihydroflavopereirine 15 and flavopereirine 9 are presented.Starting from well accessible precursors, these total syntheses highlight the preparative potential of a new method for indole synthesis based on the formation of the C2-C3 bond by low-valent titanium induced reductive coupling of oxo-amides.

A DIRECTED METALATION ROUTE TO THE ZWITTERIONIC INDOLE ALKALOIDS. SYNTHESES OF INDOLOQUINOLIZINE, FLAVOPEREIRINE, FLAVOCARPINE, AND DIHYDROFLAVOPEREIRINE

Gribble, Gordon W.,Johnson, David A.

, p. 5259 - 5262 (2007/10/02)

A protocol involving beta-lithiation of 2-(2-pyridinyl)indoles (4->5) and subsequent reaction with bromoacetaldehyde or oxirane has led to syntheses of the alkaloids indoloquinolizine (1), flavopereirine (2), flavocarpine (21), and dihydroflavopere

CONVENIENT SYNTHESIS OF 6,7-DIHYDROFLAVOPEREIRINE AND FLAVOPEREIRINE

Giri, Venkatachalam S.,Maiti, Bhim C.,Pakrashi, Satyesh C.

, p. 233 - 236 (2007/10/02)

The alkaloids 6,7-dihydroflavopereirine (9) and flavopereirine (10) have been synthesized from 3-acetyl-4-oxo-6,7-dihydro-12H-indolo-quinolizine (5) obtained in one step by condensation of 1-methyl-3,4-dihydro-β-carboline (3) and ethyl ethoxymethyleneacetoacetate (4).

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