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2,7-dichloro-9H-fluoren-9-ol is a chemical compound with the molecular formula C13H8Cl2O. It is a derivative of fluorenol, a polycyclic aromatic compound, characterized by the presence of two chlorine atoms at the 2nd and 7th positions of the fluorene ring. This white crystalline solid is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and stability, it is widely used in the chemical industry for the preparation of various products, such as dyes, pigments, and polymers. The compound is also known for its potential applications in materials science, particularly in the development of advanced materials with unique properties.

7012-24-0

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7012-24-0 Usage

Classification

Polycyclic aromatic hydrocarbon derivative

Molecular structure

Consists of a fluorene core (a polycyclic aromatic hydrocarbon) with two chlorine atoms and a hydroxyl group attached

Usage

Commonly used in the synthesis of pharmaceuticals and agrochemicals

Biological activities

Studied for its potential as an antibacterial and antifungal agent

Role in organic synthesis

Used as a building block in organic synthesis

Role in chemical reactions

Used as a reagent in chemical reactions

Unique features

Unique chemical structure that makes it useful in the development of new materials and as a potential candidate for further research in medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 7012-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7012-24:
(6*7)+(5*0)+(4*1)+(3*2)+(2*2)+(1*4)=60
60 % 10 = 0
So 7012-24-0 is a valid CAS Registry Number.

7012-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dichloro-9H-fluoren-9-ol

1.2 Other means of identification

Product number -
Other names 2,7-Dichlor-fluoren-9-ol

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7012-24-0 SDS

7012-24-0Relevant academic research and scientific papers

Strain and hueckel aromaticity: Driving forces for a promising new generation of electron acceptors in organic electronics

Brunetti,Gong,Tong,Heeger,Wudl, Fred

supporting information; experimental part, p. 532 - 536 (2010/04/24)

(Figure Presented) Straining at the leash: The main features of electron-accepting materials with a 9,9′-bifluorenylidene backbone are strain relief and a gain in aromaticity. These dimers (see picture) exhibit absorption near the red spectral region (ca. 600 nm) and HOMO (5.58-5.06 eV) and LUMO (3.37-3.09 eV) energy levels, which, together with high solubility and thermal stability render these materials attractive acceptors for bulk heterojunction (BHJ) solar cells.

Pinacolization and reduction of aromatic carbonyls with aluminium-KOH

Khurana, Jitender M.,Sehgal, Arti,Gogia, Amita,Manian, Aparna,Maikap, Golak C.

, p. 2213 - 2215 (2007/10/03)

A simple and rapid procedure for the pinacolization of aromatic aldehydes and reduction of hindered ketones with inexpensive aluminium and KOH in methanol at ambient temperature is reported. The pinacolization and reduction are proposed to be proceeding via single electron transfer from aluminium. Copyright 1996 by the Royal Society of Chemistry.

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