Home Aldehydes 4707-71-5
4707-71-5,MFCD00001175
Catalog No.:AA003TL4

4707-71-5 | Phenanthrene-9-carboxaldehyde

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250mg
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1g
97%
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$28.00   $20.00
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5g
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$97.00   $68.00
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25g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003TL4
Chemical Name:
Phenanthrene-9-carboxaldehyde
CAS Number:
4707-71-5
Molecular Formula:
C15H10O
Molecular Weight:
206.2393
MDL Number:
MFCD00001175
SMILES:
O=Cc1cc2ccccc2c2c1cccc2
NSC Number:
1932
Properties
Properties
 
BP:
405.7°C at 760 mmHg  
Form:
Solid  
MP:
100-103 °C(lit.)  
Solubility:
Soluble in acetone, dichloromethane, methanol.  
Stability:
Air Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
260  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
3.9  

Upstream Synthesis Route

[1]Tetrahedron,1997,vol.53,#43,p.14599-14614

[2]AngewandteChemie-InternationalEdition,2018,vol.57,#44,p.14593-14596

[3]Angew.Chem.,2018,vol.130,#44,p.14801-14805,5

[4]BulletinoftheChemicalSocietyofJapan,1971,vol.44,p.2237-2248

[1]Tetrahedron,1984,vol.40,#23,p.5001-5004

[2]SyntheticCommunications,1984,vol.14,#9,p.875-882

[1]SyntheticCommunications,1989,vol.19,#19,p.3385-3396

[2]SyntheticCommunications,1989,vol.19,#20,p.3469-3476

[1]Tetrahedron,1990,vol.46,#19,p.6869-6878

[2]SyntheticCommunications,1989,vol.19,#19,p.3385-3396

[1]JournalofOrganicChemistry,1983,vol.48,#5,p.749-751

Downstream Synthesis Route
5343-35-1    4707-71-5   
1-(9phenanthrylmethyl-amino)-pentan-2-ol 

[1]May[JournalofOrganicChemistry,1946,vol.11,p.353,354,357]

[1]AngewandteChemie-InternationalEdition,2006,vol.45,p.6718-6722

[2]BulletinoftheChemicalSocietyofJapan,1997,vol.70,p.156-168

[3]EuropeanJournalofMedicinalChemistry,2020,vol.202

[4]Tetrahedron,2001,vol.57,p.2871-2884

[5]InorganicChemistry,2017,vol.56,p.13715-13731

[6]BulletinoftheChemicalSocietyofJapan,1995,vol.68,p.2595-2602

[7]OrganicLetters,2007,vol.9,p.5429-5432

[8]EuropeanJournalofOrganicChemistry,2011,p.942-950

[9]SyntheticCommunications,1992,vol.22,p.497-507

[10]JournaloftheAmericanChemicalSociety,1933,vol.55,p.2995,2996

[11]JournalofOrganicChemistry,1966,vol.31,p.95-99

[12]SyntheticCommunications,1992,vol.22,p.497-507

[13]Macromolecules,2013,vol.46,p.1939-1947

[14]ChemicalCommunications,2015,vol.51,p.7610-7613

[15]PhotochemicalandPhotobiologicalSciences,2017,vol.16,p.925-934

[1]Journalofmedicinalchemistry,1964,vol.7,p.824-826

[1]SpectrochimicaActaPartA:MolecularandBiomolecularSpectroscopy,2017,vol.175,p.168-176

[2]JournalofOrganicChemistry,1971,vol.36,p.3539-3541

[1]Tetrahedron,1997,vol.53,p.14599-14614

[2]AngewandteChemie-InternationalEdition,2018,vol.57,p.14593-14596    Angew.Chem.,2018,vol.130,p.14801-14805,5

[3]BulletinoftheChemicalSocietyofJapan,1971,vol.44,p.2237-2248

Literature

Title: Expedient synthesis and structure-activity relationships of phenanthroindolizidine and phenanthroquinolizidine alkaloids.

Journal: Organic & biomolecular chemistry 20060307

Title: The study on the synthesis and the effects on the intracellular calcium of some 9-substituted-phenanthrene derivatives.

Journal: Bollettino chimico farmaceutico 20040401

Title: Disposable amperometric immunosensor for the detection of polycyclic aromatic hydrocarbons (PAHs) using screen-printed electrodes.

Journal: Biosensors & bioelectronics 20030101

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