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1573-92-8,MFCD00011537
Catalog No.:AA001PAC

1573-92-8 | 9-Fluorenone-1-carboxylic acid

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Purity
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1g
>98.0%(T)(HPLC)
in stock  
$58.00   $40.00
- +
5g
>98.0%(T)(HPLC)
in stock  
$172.00   $120.00
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25g
95%
in stock  
$809.00   $567.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001PAC
Chemical Name:
9-Fluorenone-1-carboxylic acid
CAS Number:
1573-92-8
Molecular Formula:
C14H8O3
Molecular Weight:
224.2115
MDL Number:
MFCD00011537
SMILES:
O=C1c2c(cccc2c2c1cccc2)C(=O)O
NSC Number:
24049
Properties
Properties
 
BP:
461.6°C at 760 mmHg  
Form:
Solid  
MP:
196-198 °C(lit.)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
349  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.6  

Downstream Synthesis Route

[1]Fittig;Liepmann[JustusLiebigsAnnalenderChemie,1880,vol.200,p.3]Fittig;Gebhard[JustusLiebigsAnnalenderChemie,1878,vol.193,p.148]

[2]Bapat,JayantB.;Brown,RogerF.C.;Bulmer,GlennH.;Childs,Trevor;Coulston,KarenJ.;Eastwood,FrankW.;Taylor,DennisK.[AustralianJournalofChemistry,1997,vol.50,#12,p.1159-1182]

[1]Forrest;Tucker[JournaloftheChemicalSociety,1948,p.1137,1140]

[2]BERGMANN;ORCHIN[JournaloftheAmericanChemicalSociety,1949,vol.71,#3,p.1111-1111]

[3]Fittig;Liepmann[JustusLiebigsAnnalenderChemie,1880,vol.200,p.13]

[4]Morrison[JournalofOrganicChemistry,1958,vol.23,p.1772]

[5]Cairns,J.F.;Hickinbottom,W.J.[JournaloftheChemicalSociety,1962,p.867-870]

[6]CurrentPatentAssignee:TEVAPHARMACEUTICALINDUSTRIESLTD.-EP1589016,2005,A1Locationinpatent:Page/Pagecolumn26

[1]ChemischeBerichte,1924,vol.57,p.317

[1]ChemischeBerichte,1924,vol.57,p.317

[1]Mayer;Freitag[ChemischeBerichte,1921,vol.54,p.354]

Literature

Title: Substrate specificity and structural characteristics of the novel Rieske nonheme iron aromatic ring-hydroxylating oxygenases NidAB and NidA3B3 from Mycobacterium vanbaalenii PYR-1.

Journal: mBio 20100101

Title: Bacterial degradation of aromatic compounds.

Journal: International journal of environmental research and public health 20090101

Title: Metabolism of fluoranthene by Mycobacterium sp. strain AP1.

Journal: Applied microbiology and biotechnology 20060501

Title: Metabolism of fluoranthene by mycobacterial strains isolated by their ability to grow in fluoranthene or pyrene.

Journal: Journal of industrial microbiology & biotechnology 20051001

Title: Practical synthesis of an open geodesic polyarene with a fullerene-type 6:6-double bond at the center: diindeno[1,2,3,4-defg;1',2',3',4'-mnop]chrysene.

Journal: Journal of the American Chemical Society 20020731

Title: Utilization of mixtures of polycyclic aromatic hydrocarbons by bacteria isolated from contaminated sediment.

Journal: FEMS microbiology ecology 20020701

Title: Fluoranthene degradation in Pseudomonas alcaligenes PA-10.

Journal: Biodegradation 20010101

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SDS
Tags:1573-92-8 Molecular Formula|1573-92-8 MDL|1573-92-8 SMILES|1573-92-8 9-Fluorenone-1-carboxylic acid