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9-phenyl-9H-fluoren-9-amine is an organic compound with the molecular formula C19H15N and a molecular weight of 259.33 g/mol. It is a derivative of fluorene, a polycyclic aromatic hydrocarbon, and features a phenyl group attached to the fluorene core. This chemical is known for its potential applications in the synthesis of various materials, such as polymers and pharmaceuticals, due to its unique structure and reactivity. It is typically synthesized through various chemical reactions and can be used as a building block for more complex molecules. The compound is also of interest in research for its potential properties and reactivity, which can be explored for new applications in chemistry and materials science.

6277-86-7

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6277-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6277-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6277-86:
(6*6)+(5*2)+(4*7)+(3*7)+(2*8)+(1*6)=117
117 % 10 = 7
So 6277-86-7 is a valid CAS Registry Number.

6277-86-7SDS

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 9-phenylfluoren-9-amine

1.2 Other means of identification

Product number -
Other names 9-Amino-9-phenyl-fluoren

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:6277-86-7 SDS

6277-86-7Relevant academic research and scientific papers

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0109; 0111; 0115-0116, (2020/11/28)

The compound is represented by chemical formula 1. 1 Is a cross-sectional view of an organic electronic device including an organic material layer between the first electrode, the first 2 electrode and the first 1 electrode, and 2. A compound represented

Rhodium-catalyzed intramolecular dehydrogenative aryl-aryl coupling using air as terminal oxidant

Baars, Hannah,Unoh, Yuto,Okada, Takeshi,Hirano, Koji,Satoh, Tetsuya,Tanaka, Ken,Bolm, Carsten,Miura, Masahiro

supporting information, p. 1782 - 1784 (2015/02/19)

Intramolecular dehydrogenative cyclization involving twofold Csp2-H bond cleavages directed by the amino- or carboxy group proceeds smoothly when using a rhodium-copper catalyst system under air as the terminal oxidant. A variety of fluorene derivatives can be prepared by the environmentally benign procedure.

Unexpected cyclization of tritylamines promoted by copper salt through c-h and c-n bond cleavages to produce acridine derivatives

Morioka, Ryosuke,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

, p. 12720 - 12724 (2015/03/30)

Herein, we demonstrate that tritylamines undergo an unprecedented copper-mediated cyclization involving the cleavages of two C-H bonds and one C-N bond to give 9-arylacridine derivatives. This kind of acridines is of interest due to their biological properties and their unique optical and electro- and photochemical properties. Some of obtained acridine derivatives exhibit intense fluorescence in the solid state.

Synthesis of fluorene derivatives through rhodium-catalyzed dehydrogenative cyclization

Morimoto, Keisuke,Itoh, Masaki,Hirano, Koji,Satoh, Tetsuya,Shibata, Yu,Tanaka, Ken,Miura, Masahiro

supporting information; experimental part, p. 5359 - 5362 (2012/06/18)

Doubling up: Two C-H bond activations took place efficiently upon treatment of 1 with a rhodium catalyst to form dehydrogenative cyclization products 2. Furthermore, 3 undergoes similar cyclization and subsequent decarboxylation through the cleavage of two C-H bonds and one C-C bond. Both reactions provide straightforward routes to the fluorene framework. Copyright

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