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7471-95-6

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7471-95-6 Usage

Description

9H-Fluorene-9-carboxylic acid amide is a chemical compound derived from Fluorene, a polycyclic aromatic hydrocarbon known as a micropollutant. It is characterized by its unique structure and properties, making it a versatile molecule for various applications.

Uses

Used in Chemical Synthesis:
9H-Fluorene-9-carboxylic acid amide is used as a building block in the synthesis of various organic compounds and pharmaceuticals. Its amide functionality allows for the formation of amides, esters, and other derivatives, contributing to the development of new molecules with potential applications in different fields.
Used in Material Science:
In the field of material science, 9H-Fluorene-9-carboxylic acid amide is utilized as a precursor for the development of advanced materials, such as polymers and coatings. Its aromatic structure and amide group enable the creation of materials with improved properties, such as enhanced stability, durability, and performance.
Used in Environmental Remediation:
9H-Fluorene-9-carboxylic acid amide can be employed as a component in the design of environmental remediation strategies. Its ability to interact with other molecules and form complexes can be leveraged to remove pollutants and contaminants from the environment, contributing to cleaner and safer ecosystems.
Used in Research and Development:
As a derivative of Fluorene, 9H-Fluorene-9-carboxylic acid amide is also used in research and development to study the properties and behavior of polycyclic aromatic hydrocarbons. This knowledge can be applied to develop new methods for detecting, monitoring, and mitigating the impact of these micropollutants on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 7471-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7471-95:
(6*7)+(5*4)+(4*7)+(3*1)+(2*9)+(1*5)=116
116 % 10 = 6
So 7471-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO/c15-14(16)13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13H,(H2,15,16)

7471-95-6SDS

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 9H-fluorene-9-carboxamide

1.2 Other means of identification

Product number -
Other names 9-fluorenecarboxamide

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:7471-95-6 SDS

7471-95-6Relevant articles and documents

The impact of cation structure upon the acidity of triazolium salts in dimethyl sulfoxide

Konstandaras, Nicholas,Dunn, Michelle H.,Guerry, Max S.,Barnett, Christopher D.,Cole, Marcus L.,Harper, Jason B.

supporting information, p. 66 - 75 (2019/12/26)

A series of triazolium salts, selected for their varying electronic and steric properties, were prepared and their pKa values were determined in DMSO at 25 °C using the bracketing indicator method. The effect of each systematic structural variation upon the acidity of the triazolium cation has been considered, in particular examining the effects of systematically altering electronic properties, quantified through the use of Hammett σ parameters. The first pKa value for an azolium salt that generates a mesionic carbene is also reported. These new data allow for the selection of appropriate bases for the deprotonation of such triazolium salts and the potential to correlate the pKa values determined herein with the nucleophilicity of the corresponding carbenes.

Anti-viral method

-

, (2008/06/13)

PCT No. PCT/US97/07431 Sec. 371 Date Jan. 6, 1999 Sec. 102(e) Date Jan. 6, 1999 PCT Filed May 2, 1997 PCT Pub. No. WO97/41846 PCT Pub. Date Nov. 13, 1997The present invention provides compounds which inhibit an envelope virus by inhibiting the fusion of the virus with the host cell. The virus may be inhibited in an infected cell, a cell susceptible of infection or a mammal in need thereof.

Treating cardiac arrhythmias

-

, (2008/06/13)

Fluorenes bearing a 9-aminoalkyl substituent are useful antiarrhythmic agents. Pharmaceutical formulations containing such compounds are provided, as well as a method of treatment.

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