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15860-31-8

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15860-31-8 Usage

General Description

9H-fluoren-2-yl(phenyl)methanone is a chemical compound with the molecular formula C20H14O. It is a ketone derivative with a fluorenyl group attached to a phenyl group. 9H-fluoren-2-yl(phenyl)methanone is commonly used in organic synthesis and has been studied for its potential applications in pharmaceuticals and materials science. It exhibits interesting chemical reactivity and has been found to participate in various types of organic reactions, making it a useful building block for the synthesis of complex organic molecules. Additionally, it has also been investigated for its potential biological activities and is of interest to researchers in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 15860-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15860-31:
(7*1)+(6*5)+(5*8)+(4*6)+(3*0)+(2*3)+(1*1)=108
108 % 10 = 8
So 15860-31-8 is a valid CAS Registry Number.

15860-31-8SDS

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 9H-fluoren-2-yl(phenyl)methanone

1.2 Other means of identification

Product number -
Other names fluoren-2-yl-phenyl ketone

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:15860-31-8 SDS

15860-31-8Relevant articles and documents

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Perrier

, p. 591 (1903)

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Erbium trifluoromethanesulfonate catalyzed Friedel-Crafts acylation using aromatic carboxylic acids as acylating agents under monomode-microwave irradiation

Tran, Phuong Hoang,Hansen, Poul Erik,Nguyen, Hai Truong,Le, Thach Ngoc

, p. 612 - 618 (2015/02/19)

Erbium trifluoromethanesulfonate is found to be a good catalyst for the Friedel-Crafts acylation of arenes containing electron-donating substituents using aromatic carboxylic acids as the acylating agents under microwave irradiation. An effective, rapid and waste-free method allows the preparation of a wide range of aryl ketones in good yields and in short reaction times with minimum amounts of waste.

N-Acylimidazoles-Trifluoroacetic Acid System as the Acylating Agent for Aromatic Hydrocarbons

Keumi, Takashi,Saga, Hiroshi,Kitajima, Hidehiko

, p. 1638 - 1641 (2007/10/02)

N-Benzoylimidazole in trifluoroacetic acid could benzoylate electron-rich aromatic compounds, such as durene, p-dimethoxybenzene, mesitylene, anisole, thiophene, and fluorene, to give the corresponding benzophenone derivatives in good yields.It was further elucidated, in the reaction of fluorene, that N-acylimidazoles composed of a variety of acyl groups also could be used for the ketone synthesis.Therein, the imidazolides of aliphatic carboxylic acids or substituted benzoic acid with an electron-donating group gave ketones in high yields.The above-mentioned aromaticcompounds were also acylated with N-trifluoroacetylimidazole and free carboxylic acids in trifluoroacetic acid.The mechanism for these reactions was assumed to proceed via a mixed anhydride between trifluoroacetic acid.

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