Home Other Building Blocks 62803-47-8
62803-47-8,MFCD00513530
Catalog No.:AA003N5K

62803-47-8 | 6-Hydroxy-1-indanone

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Purity
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250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$12.00   $8.00
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5g
98%
in stock  
$32.00   $22.00
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10g
98%
in stock  
$57.00   $40.00
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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:
AA003N5K
Chemical Name:
6-Hydroxy-1-indanone
CAS Number:
62803-47-8
Molecular Formula:
C9H8O2
Molecular Weight:
148.1586
MDL Number:
MFCD00513530
SMILES:
Oc1ccc2c(c1)C(=O)CC2
Properties
Properties
 
BP:
329°C at 760 mmHg  
Form:
Solid  
MP:
154-158 °C(lit.)  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
176  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
1.3  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,2018,vol.83,#1,p.452-458

[2]BioorganicandMedicinalChemistryLetters,2018,vol.28,#14,p.2436-2441

[1]TetrahedronLetters,1983,vol.24,#30,p.3095-3098

[2]TetrahedronLetters,1983,vol.24,#30,p.3095-3098

[1]OrganicPreparationsandProceduresInternational,2009,vol.41,#4,p.309-314

[2]JournalofMedicinalChemistry,1998,vol.41,#7,p.1068-1083

[3]BioorganicandMedicinalChemistryLetters,2007,vol.17,#20,p.5665-5670

[4]BioorganicandMedicinalChemistryLetters,2007,vol.17,#6,p.1675-1678

[5]ChemicalCommunications,2011,vol.47,#22,p.6290-6292

[6]OrganicandBiomolecularChemistry,2017,vol.15,#35,p.7374-7379

[7]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1984,#4,p.687-695

[8]TetrahedronLetters,1997,vol.38,#50,p.8749-8752

[9]Patent:WO2009/5998,2009,A1,.Locationinpatent:Page/Pagecolumn266

[10]EuropeanJournalofOrganicChemistry,2003,#9,p.1681-1686

[11]Patent:US6166006,2000,A,

[12]MolecularCrystalsandLiquidCrystals,2011,vol.545,p.149-155

[13]EuropeanJournalofMedicinalChemistry,2018,vol.148,p.487-497

[14]Patent:US2820817,1954,,

[1]ChemicalCommunications,2011,vol.47,#23,p.6635-6637

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1984,#4,p.687-695

[2]ChemicalCommunications,2011,vol.47,#22,p.6290-6292

[3]MolecularCrystalsandLiquidCrystals,2011,vol.545,p.149-155

[4]OrganicandBiomolecularChemistry,2017,vol.15,#35,p.7374-7379

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1923,vol.123,p.1482,1508

[2]Farmaco,EdizioneScientifica,1983,vol.38,p.167-172

62803-47-8    2146-61-4   
6-2-(3-methoxyphenyl)ethoxy-1-indanone 

[1]Lathioor,EdwardC.;Leigh,WilliamJ.[CanadianJournalofChemistry,2001,vol.79,#12,p.1851-1863]

62803-47-8    4455-09-8   
6-2-(phenyl)ethoxy-1-indanone 

[1]CanadianJournalofChemistry,2001,vol.79,p.1851-1863

[1]Patent:US2007/265332,2007,A1.Locationinpatent:Page/Pagecolumn33-34

[1]Ferranti,A.;Garuti,L.;Giovanninetti,G.;Brigidi,P.[Farmaco,EdizioneScientifica,1983,vol.38,#3,p.167-172]

[2]Ingold;Piggott[JournaloftheChemicalSociety,1923,vol.123,p.1482,1508]

[3]Ingold;Piggott[JournaloftheChemicalSociety,1923,vol.123,p.1482,1508]

Literature

Title: 1-[3-(4-Nitro-phen-yl)propano-yl]urea acetic acid monosolvate.

Journal: Acta crystallographica. Section E, Structure reports online 20111101

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