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5H-Naphtho[2,3-a]carbazole-5,13(12H)-dione is a complex organic compound with the molecular formula C19H11NO2. It is a derivative of the naphtho[2,3-a]carbazole family, characterized by its unique fused-ring structure. 5H-Naphtho[2,3-a]carbazole-5,13(12H)-dione is known for its potential applications in the field of pharmaceuticals and materials science, particularly due to its interesting chemical properties and the possibility of it being a precursor to other more complex molecules. The specific structure, with two carbonyl groups at positions 5 and 13, gives it distinct reactivity and stability, which can be exploited in various chemical transformations. Research into compounds like this often focuses on their synthesis, potential therapeutic applications, and physical-chemical characteristics, making it a subject of interest for chemists and material scientists.

7600-14-8

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7600-14-8 Usage

Abbreviation

NCBD

Chemical Class

Polycyclic aromatic compound

Physical State

Yellow crystalline solid

Molecular Weight

335.34 g/mol

Applications

Organic Synthesis: Used in various research fields
Material Science: Utilized for its unique structure and properties

Potential Uses

Building Block for Organic Semiconductor Materials: Used in optoelectronic devices like OLEDs and organic solar cells
Fluorescent Probe: Demonstrated potential for detecting nitric oxide (NO) in biological systems

Check Digit Verification of cas no

The CAS Registry Mumber 7600-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7600-14:
(6*7)+(5*6)+(4*0)+(3*0)+(2*1)+(1*4)=78
78 % 10 = 8
So 7600-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H11NO2/c22-19-13-6-1-2-7-14(13)20(23)17-15(19)10-9-12-11-5-3-4-8-16(11)21-18(12)17/h1-10,21H

7600-14-8Downstream Products

7600-14-8Relevant academic research and scientific papers

THE 3-VINYLINDOLE PARENT COMPOUND AND ITS ANION: NEW REACTIVITY ASPECTS

Pindur, Ulf,Kim, Myung-Hwa,Eitel, Manfred

, p. 1551 - 1552 (2007/10/02)

Synthesis and reactivity of the parent 3-vinylindole and its anion are described.These compounds react as dienes in HOMOdiene-controlled Diels-Alder reactions.In the presence of dichloromethane, the 3-vinylindole undergoes an SN reaction to furnish a dimeric product.

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