947-73-9

Basic information

• Product Name: 9-AMINOPHENANTHRENE
• Synonyms: 9-AMinophenathrene;9-Aminophenanthrene 96%;9-PHENANTHRENAMINE;9-AMINOPHENANTHRENE;9-Phenanthrylamine;phenanthren-9-amine;Phenanthrylamine;2-aminophenanthrene
• CAS NO: 947-73-9
• Molecular Formula: C₁₄H₁₁N
• Molecular Weight: 193.24
• EINECS: 213-431-6
• Mol File: 947-73-9.mol
• Article Data: 29

Chemical Properties

• Melting Point: 137-139 °C(lit.)
• Boiling Point: 319.47°C (rough estimate)
• Flash Point: 224.4°C
• Appearance: White to brown/Solid
• Density: 1.1061 (rough estimate)
• Vapor Pressure: 7.12E-07mmHg at 25°C
• Refractive Index: 1.5850 (estimate)
• PKA: 4.32±0.30(Predicted)
• Water Solubility: It is slightly soluble in water 0.00581 mg/mL.
• CAS DataBase Reference: 9-AMINOPHENANTHRENE(CAS DataBase Reference)
• NIST Chemistry Reference: 9-AMINOPHENANTHRENE(947-73-9)
• EPA Substance Registry System: 9-AMINOPHENANTHRENE(947-73-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• RTECS: SG0175000
• Hazardous Substances Data: 947-73-9(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 947-73-9 differently. You can refer to the following data:
1. 9-Aminophenanthrene can be used as a model ligand to study the binding of 9-aminophenanthrene to individual subsites within the active site of CYP(eryF). It is also used as a fluorescent-labeling reagent for free fatty acids (FFA),examination through HPLC.
2. 9-Aminophenanthrene was used as a model ligand to study the binding of 9-aminophenanthrene to individual subsites within the active site of CYP(eryF).

InChI:InChI=1/C14H11N/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H,15H2

Upstream product

• 2039-77-2 9-acetylphenanthrene 
• 573-17-1 9-bromophenanthrene 
• 19853-10-2 2-(biphenyl-2-yl)acetonitrile 
• 484-17-3 9-Phenanthrol 
• 4235-09-0 9-(N-acetylamino)phenanthrene 
• 5968-55-8 9-acetylphenanthrenoxime 
• 67464-46-4 1a,9b-dihydro-1H-phenanthro<9,10-b>azirine 
• 85-01-8 phenanthrene 
• 85657-96-1 trifluoroacetyl-9-aminophenanthrene 
• 75-05-8 acetonitrile 
• 107-12-0 propiononitrile 
• 7664-41-7 ammonia 
• 954-46-1 9-nitrophenanthrene 
• 10034-85-2 hydrogen iodide 

Downstream Products

• 302595-31-9 benzylidene-[9]phenanthryl-amine 
• 28820-48-6 N-[9]phenanthryl-benzenesulfonamide 
• 217-65-2 dibenzo[f,h]quinoline 
• 201-67-2 13H-13-aza-indeno[1,2-l]phenanthrene 
• 947-72-8 9-chlorophenanthrene 
• 16269-40-2 N-9-phenanthrenyl-9-phenanthrenamine 
• 88090-59-9 9H-tetrabenzocarbazole 
• 81593-08-0 N-9-phenanthrenylbenzamide 
• 4235-09-0 9-(N-acetylamino)phenanthrene 
• 87995-55-9 N-(10-Brom-9-phenanthryl)-N-methylbenzamid 
• 87995-54-8 N-(10-Brom-9-phenanthryl)benzamid 
• 87995-56-0 10-(Methylamino)-9-phenanthrophenon 
• 488829-83-0 Phenanthren-9-yl-[1-phenyl-meth-(E)-ylidene]-amine 
• 3920-79-4 N-phenyl-N-(9-phenanthryl)amine 

Relevant articles and documents

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MONO AMINE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICE INCLUDING THE SAME

An organic electroluminescent device includes a monoamine derivative represented by Formula 1: In Formula 1, Ar1 may be represented by Formula 2; Ar2 may be a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, wherein the substituent of Ar2 is an unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring; Ar1 and Ar2 may be different from each other; m may be an integer from 0 to 4; and R1 may be a substituted or unsubstituted aryl group having 6 to 30 carbon atoms for forming a ring, and when m is 2 or more, a plurality of R1 may combine to form a ring:

Direct conversion of phenols into primary anilines with hydrazine catalyzed by palladium

Primary anilines are essential building blocks to synthesize various pharmaceuticals, agrochemicals, pigments, electronic materials, and others. To date, the syntheses of primary anilines mostly rely on the reduction of nitroarenes or the transition-metal-catalyzed Ullmann, Buchwald-Hartwig and Chan-Lam cross-coupling reactions with ammonia, in which non-renewable petroleum-based chemicals are typically used as feedstocks via multiple step syntheses. A long-standing scientific challenge is to synthesize various primary anilines directly from renewable sources. Herein, we report a general method to directly convert a broad range of phenols into the corresponding primary anilines with the cheap and widely available hydrazine as both amine and hydride sources with simple Pd/C as the catalyst.

Material for organic electroluminescent device and organic electroluminescent device using the same

A material for an organic electroluminescent device and an organic electroluminescent device including the same, the material including a monoamine compound represented by the following Formula 1: