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1514-16-5

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1514-16-5 Usage

Fluorenone derivative

Contains a fluorene ring system with a ketone and a fluorine atom attached to it.

Fluorinating agent

Commonly used in organic synthesis to introduce a fluorine atom into organic molecules.

Reactions

Participates in reactions such as the Hiyama coupling.

Precursor

Used as a precursor for the synthesis of various fluorinated compounds.

Applications

Pharmaceutical and agrochemical industries.

Development

Valuable tool in the development of new fluorine-containing compounds.

Fields of application

Medicine, materials science, and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1514-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1514-16:
(6*1)+(5*5)+(4*1)+(3*4)+(2*1)+(1*6)=55
55 % 10 = 5
So 1514-16-5 is a valid CAS Registry Number.

1514-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluorofluoren-9-one

1.2 Other means of identification

Product number -
Other names 9H-Fluoren-9-one,1-fluoro

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:1514-16-5 SDS

1514-16-5Relevant articles and documents

Synthesis of fluorenones through rhodium-catalyzed intramolecular acylation of biarylcarboxylic acids

Fukuyama, Takahide,Maetani, Shinji,Miyagawa, Kazusa,Ryu, Ilhyong

supporting information, p. 3216 - 3219 (2014/07/08)

An efficient approach to the synthesis of fluorenones via the rhodium-catalyzed intramolecular acylation of biarylcarboxylic acids was developed. Using this procedure, fluorenones with various substituents can be synthesized in good to high yields. This work marks the first recorded use of catalytic intramolecular acylation to synthesize fluorenones.

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