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2969-67-7

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2969-67-7 Usage

General Description

2,4,7-trifluoro-9H-fluoren-9-one is a chemical compound with the molecular formula C13H6F3O. It is a fluorinated derivative of fluorenone, a tricyclic aromatic ketone. 2,4,7-trifluoro-9H-fluoren-9-one is used in the field of organic synthesis and materials chemistry as a building block for the production of various other fluorinated compounds. It has also been used as a research reagent in the study of fluorine-containing compounds and their properties. Additionally, its unique chemical structure and properties make it a valuable tool for the development of new pharmaceuticals, agrochemicals, and other specialized chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 2969-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2969-67:
(6*2)+(5*9)+(4*6)+(3*9)+(2*6)+(1*7)=127
127 % 10 = 7
So 2969-67-7 is a valid CAS Registry Number.

2969-67-7SDS

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 2,4,7-trifluorofluoren-9-one

1.2 Other means of identification

Product number -
Other names 2,4,7-trifluoro-9h-fluoren-9-one

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:2969-67-7 SDS

2969-67-7Downstream Products

2969-67-7Relevant articles and documents

A General Synthesis of Substituted Fluorenones and Azafluorenones

Kyba, Evan P.,Liu, Shiuh-Tzung,Chockalingam, Kannappan,Reddy, B. Raghava

, p. 3513 - 3521 (2007/10/02)

Twenty-one variously substituted fluorenones and azafluorenones have been synthesized via photochemical Pschorr cyclizations of 2-diazoniodiaryl ketones as the key ring-forming step.Direct, (bipy)3RuII-, or (bipy)3RuII/CuII-photosensitized conditions were used, depending on the system to be cyclized.Where selectivities were possible in the ring closure, the isomer ratios obtained were in accord with an aryl radical as the reactive intermediate.The precursor aminodiaryl ketones were obtained from the sequence ortho lithiation of an arylpivalamide, reaction withan aryl aldehyde to give a 2-pivalamidodiarylcarbinol, oxidation to give a 2-pivalamidodiaryl ketone, and hydrolysis to give the 2-aminodiaryl ketone.

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