6276-05-7

Basic information

• Product Name: 3-AMINO-9-FLUORENONE
• Synonyms: 3-AMINO-9-FLUORENONE;TIMTEC-BB SBB000340;2-Methyl-3-nitrobiphenyl;3-amino-9H-fluoren-9-one
• CAS NO: 6276-05-7
• Molecular Formula: C₁₃H₉NO
• Molecular Weight: 195.22
• Product Categories: C13 to C14;Carbonyl Compounds;Ketones
• Mol File: 6276-05-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 154-155 °C(lit.)
• Boiling Point: 422.6 °C at 760 mmHg
• Flash Point: 209.4 °C
• Appearance: /
• Density: 1.327g/cm³
• Vapor Pressure: 2.38E-07mmHg at 25°C
• Refractive Index: 1.72
• PKA: 1.77±0.20(Predicted)
• CAS DataBase Reference: 3-AMINO-9-FLUORENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-9-FLUORENONE(6276-05-7)
• EPA Substance Registry System: 3-AMINO-9-FLUORENONE(6276-05-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• Hazardous Substances Data: 6276-05-7(Hazardous Substances Data)

Usage

General Description

3-AMINO-9-FLUORENONE is a chemical compound consisting of a fluorenone core with an amino group located at the third position. It is commonly used as a fluorescent probe and as a building block for various organic synthesis reactions. 3-AMINO-9-FLUORENONE has been studied for its potential applications in organic electronics, as well as in the development of new materials for optical and sensor technologies. 3-AMINO-9-FLUORENONE has also been investigated for its potential use in medicinal chemistry, with research focusing on its antioxidant and anti-inflammatory properties. Overall, this chemical compound has a wide range of potential applications in various scientific and industrial fields.

InChI:InChI=1/C13H9NO/c14-8-5-6-11-12(7-8)9-3-1-2-4-10(9)13(11)15/h1-7H,14H2

Upstream product

• 486-25-9 9-fluorenone 
• 42135-22-8 3-nitro-9H-fluoren-9-one 

Downstream Products

• 343-40-8 3-fluoro-9H-fluorene 
• 1514-15-4 3-fluoro-9-fluorenone 
• 6098-47-1 3-(methylthio)-2-acetamidofluorene 
• 16233-24-2 3-Methylmercapto-9-oxo-fluoren-S-oxid 
• 16233-23-1 3-Methylmercapto-fluorenon 
• 16233-05-9 2-Nitro-3-methylmercapto-fluoren 
• 3096-56-8 2-bromofluoren-9-one 
• 318-12-7 6-Fluor-2-amino-fluorenon-(9); =3-Fluor-7-amino-fluorenon-(9) 
• 16233-22-0 Dithiokohlensaeure-O-ethylester-S-<9-oxo-fluorenyl-(3)-ester> 
• 7247-90-7 9-hydroxy-3-aminofluorene 
• 6276-06-8 N-(9-oxo-fluoren-3-yl)-acetamide 
• 6344-66-7 9H-fluoren-3-amine 

Relevant articles and documents

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Containing 3 mono-substituted or 3,6 di substituted fluorenyl metallocene and its preparation method and application (by machine translation)

The invention relates to a 3 mono-substituted or 3,6 b-substituted fluorene derivatives and [...] with the framework and the cross-linked metallocene compound and its preparation method and application. Wherein the preparation method comprises the following steps : (1) 3 mono-substituted or 3,6 di-substituted [...][...] in ether with the reaction to prepare fluorenyl/indenyl ligands lithium salt, (2) let fluorenyl/indenyl ligands of lithium salts with alkyl, alkenyl or an organic silyl halide reaction, in order to get the indenyl group in the 3 position with corresponding alkyl, alkenyl or an organic silyl halides of bridge fluorenyl/indenyl ligands ; (3) and a metal compound ligand the reaction may be carried out to obtain the corresponding metal complex metal cyclopentadienyl. The invention discloses a novel fluorenyl metallocene; the preparation method of this invention the synthetic steps are brief, the operation is simple, high yield, raw materials are easy, low cost, environmental pollution is small, is easy for industrial production. (by machine translation)

3-monosubstituted or 3,6-disubstituted fluorene derivative and preparing method and application thereof

The invention relates to a 3-monosubstituted or 3,6-disubstituted fluorene derivative and a preparing method and application thereof. The preparing method includes the steps that fluorenone is used as a raw material for generating a 9-fluorenone nitro derivative and a 9-fluorenone amino derivative, a diazo-reaction is carried out, an electrophilic substitution or cracking reaction is carried out to generate a 3-monosubstituted or 3,6-disubstituted 9-fluorenone derivative, and the 3-monosubstituted or 3,6-disubstituted 9-fluorenone derivative is reduced to generate the 3-monosubstituted or 3,6-disubstituted fluorene derivative. The preparing method includes simple and short synthesis steps, and is moderate in reaction condition, easy to operate, high in yield, low in cost and small in environment pollution, the raw material is easy to obtain, and industrial production is easy to realize.