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2235-15-6,MFCD00156651
Catalog No.:AA003DT6

2235-15-6 | 1-Acenaphthenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$14.00   $10.00
- +
1g
98%
in stock  
$32.00   $22.00
- +
5g
98%
in stock  
$57.00   $40.00
- +
10g
98%
in stock  
$102.00   $71.00
- +
25g
98%
in stock  
$211.00   $148.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003DT6
Chemical Name:
1-Acenaphthenone
CAS Number:
2235-15-6
Molecular Formula:
C12H8O
Molecular Weight:
168.1913
MDL Number:
MFCD00156651
SMILES:
O=C1Cc2c3c1cccc3ccc2
Properties
Properties
 
BP:
337.1°C at 760 mmHg  
Form:
Solid  
MP:
122 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
233  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
XLogP3:
2.6  

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1954,p.4306,4311

[2]CanadianJournalofChemistry,1968,vol.46,p.715-728

[3]Patent:US6667303,2003,B1.Locationinpatent:Pagecolumn43

[4]Patent:WO2014/106238,2014,A1

[5]JournaloftheAmericanChemicalSociety,2014,vol.136,p.15493-15496

[6]Patent:EP1491212,2004,A1

[1]Rule;Thompson[JournaloftheChemicalSociety,1937,p.1761]

[1]TetrahedronLetters,2019,vol.60,p.931-935

[2]ChemistryLetters,2001,p.922-923

[3]BulletinoftheChemicalSocietyofJapan,2004,vol.77,p.1905-1914

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1990,vol.29,p.1012-1016

[5]ACSCatalysis,2018,vol.8,p.5425-5430

[6]JournaloftheChemicalSociety.PerkintransactionsI,1996,p.2451-2459

[7]JournaloftheAmericanChemicalSociety,2001,vol.123,p.4189-4196

[8]JournaloftheAmericanChemicalSociety,1940,vol.62,p.432,434

[9]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1926,vol.182,p.1228

[10]AustralianJournalofChemistry,1996,vol.49,p.793-800

[11]EuropeanJournalofMedicinalChemistry,2009,vol.44,p.2563-2571

[12]BiochemicalPharmacology,2013,vol.86,p.1366-1375

[13]JournalofBiochemistry,2015,vol.158,p.425-434

[14]EuropeanJournalofOrganicChemistry,2020,vol.2020,p.4878-4885

[1]Synthesis,1989,p.293-295

[2]BulletinoftheChemicalSocietyofJapan,1992,vol.65,p.2878-2880

[3]NewJournalofChemistry,2009,vol.33,p.1637-1640

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1981,vol.20,p.153-155

[5]BulletinoftheChemicalSocietyofJapan,1995,vol.68,p.2319-2326

[6]EuropeanJournalofInorganicChemistry,2016,vol.2016,p.3513-3523

[7]JournalofPhysicalOrganicChemistry,2004,vol.17,p.798-806

[8]GazzettaChimicaItaliana,1940,vol.70,p.186,189

[9]Patent:US2859247,1954,

[10]ChemicalResearchinToxicology,1999,vol.12,p.278-285

[11]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1926,vol.182,p.1228

[12]JournaloftheAmericanChemicalSociety,1940,vol.62,p.432,434

[13]JournaloftheAmericanChemicalSociety,1940,vol.62,p.432,434

[14]JustusLiebigsAnnalenderChemie,1893,vol.276,p.15

[15]SyntheticCommunications,2008,vol.38,p.2000-2010

[16]NewJournalofChemistry,2009,vol.33,p.538-544

[17]TetrahedronLetters,2012,vol.53,p.2989-2992

[18]JournalofOrganometallicChemistry,2014,vol.774,p.61-69

[19]Patent:CN107722062,2018,A.Locationinpatent:Paragraph0098;0099;0100

[20]Patent:CN108676035,2018,A.Locationinpatent:Paragraph0069;0071

[1]OrientalJournalofChemistry,2013,vol.29,p.301-304

[2]JustusLiebigsAnnalenderChemie,1896,vol.290,p.200

[3]JournaloftheChemicalSociety,1963,p.1511-1513

[4]BulletinoftheChemicalSocietyofJapan,1969,vol.42,p.181-185

[5]Patent:KR2018/74176,2018,A.Locationinpatent:Paragraph0071-0073

Literature

Title: Ethyl (1R,1'S,2'S,7a'R)-2-oxo-1'-[(3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetra-methyl-tetra-hydro-3aH-bis-[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl]-1',2',5',6',7',7a'-hexa-hydro-2H-spiro-[acenaphthyl-ene-1,3'-pyrrolizine]-2'-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20120201

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: 3'-Benzoyl-1'-methyl-4'-phenyl-spiro[acenaphthyl-ene-1(2H),2'-pyrrolidin]-2-one.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: Bacterial degradation of aromatic compounds.

Journal: International journal of environmental research and public health 20090101

Title: Ethyl 3'-cyano-1'-methyl-2-oxo-4'-phenylspiro-[acenaphthene-1,2'-pyrrolidine]-3'-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20080201

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

Journal: Applied microbiology and biotechnology 20060501

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Degradation and formation of polycyclic aromatic compounds during bioslurry treatment of an aged gasworks soil.

Journal: Environmental toxicology and chemistry 20030701

Title: New methodologies for the preparation of porphodimethenes and their conversion to trans-porphyrins with functionalized naphthyl spacers.

Journal: The Journal of organic chemistry 20010810

Title: Convergent and divergent points in catabolic pathways involved in utilization of fluoranthene, naphthalene, anthracene, and phenanthrene by Sphingomonas paucimobilis var. EPA505.

Journal: Journal of industrial microbiology & biotechnology 20010601

Title: The electron as a protecting group. 3. Generation of acenaphthyne radical anion and the determination of the heat of formation of a strained cycloalkyne.

Journal: Journal of the American Chemical Society 20010509

Title: Use of 13C nuclear magnetic resonance to assess fossil fuel biodegradation: fate of [1-13C]acenaphthene in creosote polycyclic aromatic compound mixtures degraded by bacteria.

Journal: Applied and environmental microbiology 19980401

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