Home Other Building Blocks 6217-22-7
6217-22-7,MFCD00089611
Catalog No.:AA00EIH5

6217-22-7 | Pyrene-4,5-dione

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Purity
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100mg
95%
in stock  
$131.00   $92.00
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250mg
95%
in stock  
$197.00   $138.00
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1g
95%
in stock  
$477.00   $334.00
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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:
AA00EIH5
Chemical Name:
Pyrene-4,5-dione
CAS Number:
6217-22-7
Molecular Formula:
C16H8O2
Molecular Weight:
232.2335
MDL Number:
MFCD00089611
SMILES:
O=c1c2cccc3c2c2c(c1=O)cccc2cc3
Properties
Properties
 
Form:
Solid  
MP:
296 - 298°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
362  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Polyhedron,2019,vol.170,p.412-423

[2]Chemistry-AEuropeanJournal,2022,vol.28

[3]Patent:CN108658993,2018,A.Locationinpatent:Paragraph0041;0043

[4]Chemistry-AEuropeanJournal,2020,vol.26,p.438-453

[5]JournalofMaterialsChemistryC,2019,vol.7,p.3512-3521

[6]CuihuaXuebao/ChineseJournalofCatalysis,2016,vol.37,p.153-158

[7]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.5933-5936

[8]EuropeanJournalofOrganicChemistry,2021,vol.2021,p.2013-2017

[9]DyesandPigments,2020,vol.172

[10]PhotochemistryandPhotobiology,2021,vol.97,p.301-308

[11]JournalofOrganicChemistry,2005,vol.70,p.707-708

[12]OrganicLetters,2011,vol.13,p.2240-2243

[13]Patent:US9029425,2015,B2.Locationinpatent:Page/Pagecolumn131

[14]Tetrahedron,2019,vol.75

[15]OrganicLetters,2017,vol.19,p.1382-1385

[16]OrganicLetters,2021,vol.23,p.2019-2023

[17]OrganicLetters,2008,vol.10,p.3547-3550

[18]JournalofOrganicChemistry,2017,vol.82,p.6865-6873

[19]JournalofMaterialsChemistryC,2016,vol.4,p.3809-3814

[20]ChemicalCommunications,2016,vol.52,p.7986-7989

[21]Patent:CN107056710,2017,A.Locationinpatent:Paragraph0070;0071;0072

[22]Patent:CN108148001,2018,A.Locationinpatent:Paragraph0071;0080;0081;0082

[23]JournalofMaterialsChemistryC,2019,vol.7,p.10273-10280

[24]Chemistry-AnAsianJournal,2013,vol.8,p.2111-2124

[25]OrganicLetters,2010,vol.12,p.4520-4523

[26]AngewandteChemie-InternationalEdition,2018,vol.57,p.10559-10563    Angew.Chem.,2018,vol.130,p.10719-10723,5

[27]JournalofOrganicChemistry,1959,vol.24,p.1226,1228

[28]Synthesis,1974,p.229-272

[29]JournalofOrganicChemistry,1983,vol.48,p.4198-4202

[30]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.1772-1780

[31]Patent:CN107129469,2017,A.Locationinpatent:Paragraph0082;0083;0103;0104;0108;0109

[32]Patent:CN107011267,2017,A.Locationinpatent:Paragraph0019;0080

[33]Molecules,2018,vol.23

[34]InorganicChemistryCommunications,2019,vol.100,p.129-133

[35]Patent:CN109942585,2019,A.Locationinpatent:Paragraph0054-0059

[36]DyesandPigments,2013,vol.96,p.104-115,12

[1]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.1283-1291

[2]JournalofOrganicChemistry,1959,vol.24,p.1226,1228

[1]Synthesis,1982,p.459-461

[2]JustusLiebigsAnnalenderChemie,1956,vol.599,p.81,93

[3]JournalofOrganicChemistry,1986,vol.51,p.1773-1778

[1]Chemistry-AEuropeanJournal,2022,vol.28

[2]Chemistry-AEuropeanJournal,2010,vol.16,p.11121-11132

[3]JournaloftheAmericanChemicalSociety,1987,vol.109,p.4660-4665

[4]JournalofMaterialsChemistryC,2019,vol.7,p.3512-3521

[5]Chemistry-AEuropeanJournal,2018,vol.24,p.243-250

[6]OrganicLetters,2008,vol.10,p.3547-3550

[7]Patent:US9029425,2015,B2.Locationinpatent:Page/Pagecolumn131

[8]AngewandteChemie-InternationalEdition,2017,vol.56,p.6454-6458    Angew.Chem.,2017,vol.129,p.6554-6558,5

[1]OrganicLetters,2017,vol.19,p.1382-1385

[2]OrganicLetters,2021,vol.23,p.2019-2023

[3]TetrahedronLetters,1987,vol.28,p.2057-2060

[4]OrganicLetters,2011,vol.13,p.2240-2243

[5]InorganicChemistryCommunications,2019,vol.100,p.129-133

[6]ArchivesofBiochemistryandBiophysics,2019,vol.673

Literature

Title: Aluminum complexes of the redox-active [ONO] pincer ligand.

Journal: Dalton transactions (Cambridge, England : 2003) 20120714

Title: Engineering double to quintuple stacks of a polarized aromatic in confined cavities.

Journal: Journal of the American Chemical Society 20100127

Title: Bacterial degradation of aromatic compounds.

Journal: International journal of environmental research and public health 20090101

Title: Identification of proteins induced by polycyclic aromatic hydrocarbon in Mycobacterium vanbaalenii PYR-1 using two-dimensional polyacrylamide gel electrophoresis and de novo sequencing methods.

Journal: Proteomics 20041201

Title: Evidence for the existence of PAH-quinone reductase and catechol-O-methyltransferase in Mycobacterium vanbaalenii PYR-1.

Journal: Journal of industrial microbiology & biotechnology 20041201

Title: Thermal and photochemistry of a pyrene dihydrodioxin (PDHD) and its radical cation: a photoactivated masking group for ortho-quinones.

Journal: Journal of the American Chemical Society 20041201

Title: Aldehydic DNA lesions in calf thymus DNA and HeLa S3 cells produced by bacterial quinone metabolites of fluoranthene and pyrene.

Journal: Carcinogenesis 20040901

Title: Two polycyclic aromatic hydrocarbon o-quinone reductases from a pyrene-degrading Mycobacterium.

Journal: Archives of biochemistry and biophysics 20030815

Title: The effect of aging on pyrene transformation in sediments.

Journal: Environmental toxicology and chemistry 20030101

Title: MacDonald [2 + 2]-type condensation with vicinal diketones: synthesis and properties of novel spiro-tricyclic porphodimethenes.

Journal: Organic letters 20010726

Title: Products from the incomplete metabolism of pyrene by polycyclic aromatic hydrocarbon-degrading bacteria.

Journal: Applied and environmental microbiology 20000501

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Tags:6217-22-7 Molecular Formula|6217-22-7 MDL|6217-22-7 SMILES|6217-22-7 Pyrene-4,5-dione