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"9-[(4-chlorophenyl)methylidene]-2-nitro-fluorene" is a complex organic compound characterized by a fluorene core, which is a polycyclic aromatic hydrocarbon. The molecule features a nitro group at the 2-position, which is known for its reactivity and can participate in various chemical reactions. Additionally, a 4-chlorophenyl group is attached to the fluorene through a methylene bridge, providing a chlorine atom that can be a site for further functionalization. This chemical structure may have potential applications in the synthesis of pharmaceuticals, dyes, or other specialty chemicals, although specific uses would depend on its physical and chemical properties, which are not detailed in this summary. The compound's exact role and applications would be determined by further research into its stability, reactivity, and potential interactions with other molecules.

4364-38-9

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4364-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4364-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4364-38:
(6*4)+(5*3)+(4*6)+(3*4)+(2*3)+(1*8)=89
89 % 10 = 9
So 4364-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H12ClNO2/c21-14-7-5-13(6-8-14)11-19-17-4-2-1-3-16(17)18-10-9-15(22(23)24)12-20(18)19/h1-12H

4364-38-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[(4-chlorophenyl)methylidene]-2-nitrofluorene

1.2 Other means of identification

Product number -
Other names 9-[(4-chlorophenyl)methylidene]-2-nitro-fluorene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:4364-38-9 SDS

4364-38-9Downstream Products

4364-38-9Relevant academic research and scientific papers

KF-Al2O3 induced the condensation of 2-nitrofluorene and para-substituted acetophenones with aromatic aldehydes

Yan,Sun

, p. 3809 - 3814 (2007/10/03)

In the presence of KF-Al2O3 as a solid base, 2-nitrofluorene 1 condensed with aromatic aldehydes 2a-f in methanol to give 2-nitrodibenzofulvenes 3a-f in high yield. The para-substituted acetophenones 4a-f reacted with cinnamic aldehyde to give 1, 5-diaryl-2, 4-pentadien-1-ones 6a-f in moderate yield.

Synthesis and structural assignment of 2,4′-disubstituted benzylidenefluorenes and 4′-substituted benzylidene-1-azafluorenes

Annunziata, Rita,Molteni, Valentina,Raimondi, Laura

, p. 520 - 528 (2007/10/03)

In the course of a study aimed at the investigation of edge-to-face arene-arene interactions, substituted benzylidenefluorenes 8-16 and benzylidene-1-azafluorenes 20-24 were synthesized as mixtures of E-Z-isomers. The full structural assignment of these compounds, performed by 2D NMR experiments, is described together with a study of their E-Z isomerization under equilibrating conditions. For compounds 8-16 no correlation was observed between the electron-donating or electron-withdrawing nature of the substituent groups and the E/Z equilibrium ratios. In the case of 20-24 the predominance of the E-isomers seems to depend exclusively on the N-lone pair-benzylidene ring electronic repulsion rather than on the nature of the para substituent on the aromatic ring.

Ultrasonicated condensation of indene and 2-nitrofluorene with aromatic aldehydes catalyzed by bis-(p-methoxyphenyl)telluroxide (BMPTO)

Zheng, Ming,Wang, Longcheng,Shao, Jianguo,Zhong, Qi

, p. 1751 - 1755 (2007/10/03)

The condensation of indene or 2-nitrofluorene with aromatic aldehydes catalyzed by bis-(p-methoxyphenyl)telluroxide (BMPTO) under ultrasonic wave irradiation gave corresponding fulvenes in fair to good yield.

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