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5H-Indolo[2,3-b]quinoxaline, 9-fluoro- is a chemical compound belonging to the quinoxaline family, characterized by a unique structure that fuses an indolo nucleus with a quinoxaline ring. This specific compound features a fluorine atom at the 9-position, which can significantly influence its electronic properties and reactivity. It is an important molecule in the field of medicinal chemistry, particularly for its potential applications in the development of new drugs targeting various biological pathways. The presence of the fluorine atom can enhance the lipophilicity and metabolic stability of the molecule, which are crucial factors in drug design. 5H-Indolo[2,3-b]quinoxaline, 9-fluoro- is also of interest in materials science for its potential electronic and optical properties.

1496-12-4

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1496-12-4 Usage

Fluorescent Derivative

Derived from 9H-indolo[2,3-b]quinoxaline

Usage

Organic synthesis
Pharmaceutical research

Biological Activities

Anticancer properties
Antiviral properties

Potential Applications

Photodynamic therapy for cancer treatment
Fluorescent probe for imaging cellular structures and processes

Significance

Important chemical compound
Wide range of potential applications in research and medical fields

Check Digit Verification of cas no

The CAS Registry Mumber 1496-12-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1496-12:
(6*1)+(5*4)+(4*9)+(3*6)+(2*1)+(1*2)=84
84 % 10 = 4
So 1496-12-4 is a valid CAS Registry Number.

1496-12-4Relevant academic research and scientific papers

Friedl?nder reaction/quinoxalinone-benzimidazole rearrangement sequence: Expeditious entry to diverse quinoline derivatives with the benzimidazole moieties

Mamedov, Vakhid A.,Kadyrova, Saniya F.,Zhukova, Nataliya A.,Galimullina, Venera R.,Polyancev, Fedor M.,Latypov, Shamil K.

, p. 5934 - 5946 (2015/03/30)

A protocol has been developed for the efficient synthesis of structurally diverse 4-(benzimidazol-2-yl)quinolines via reactions of 3-(2-aminophenyl)quinoxalin-2(1H)-ones and ketones, including acetone, acetophenones, 1,3-pentanedione and ethyl acetoacetat

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