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7,13-dipropyl-8H-indeno[1,2-k]fluoranthen-8-one is a complex organic compound belonging to the family of indenofluoranthenones. It is characterized by a unique molecular structure, featuring a fluoranthene core with an indene ring fused to it. The compound has two propyl groups attached at the 7th and 13th positions, and a ketone functional group at the 8th position. This chemical is known for its potential applications in various fields, such as materials science and pharmaceuticals, due to its specific properties and reactivity. However, it is essential to handle 7,13-dipropyl-8H-indeno[1,2-k]fluoranthen-8-one with care, as it may have potential health and environmental impacts, and further research is needed to fully understand its applications and safety profile.

77930-39-3

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77930-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77930-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77930-39:
(7*7)+(6*7)+(5*9)+(4*3)+(3*0)+(2*3)+(1*9)=163
163 % 10 = 3
So 77930-39-3 is a valid CAS Registry Number.

77930-39-3Downstream Products

77930-39-3Relevant academic research and scientific papers

Polycyclic Aromatic Compounds: Part II - A New Synthesis of Fluorenone & Fluorene Derivatives

Bandyopadhyay, T. K.,Bhattacharya, A. J.

, p. 750 - 752 (2007/10/02)

A large number of 1,4-disubstituted-2,3-(1',8'-naphthylene)-fluorenones (VI) and -fluorenes (V), i. e. 7,13-disubstituted-8(H)-oxo- and 8H-indenofluoranthenes have been prepared.The preferred method of the synthesis is the Diels-Alder reaction of 2,5-disubstituted-3,4-(1',8'-naphthylene)cyclopentadienones (I) with phenylpropiolic esters (II) to give fluoranthene derivatives (IV).The latter, on cyclisation and reduction yield the desired fluorenes.Phenylpropiolic acids (VII) are also added to I to give fluoranthenes (VIII) and fluoranthene-8-carboxylic acids (IX).The acids (IX) undergo smooth cyclisation to fluorenones (VI) on treatment with conc. sulphuric acid.

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