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27550-59-0,MFCD00997252
Catalog No.:AA002TZL

27550-59-0 | 5-Hydroxyisobenzofuran-1,3-dione

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$7.00   $5.00
- +
250mg
95%
in stock  
$9.00   $7.00
- +
1g
95%
in stock  
$17.00   $12.00
- +
5g
95%
in stock  
$52.00   $36.00
- +
25g
95%
in stock  
$256.00   $179.00
- +
  • 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:
AA002TZL
Chemical Name:
5-Hydroxyisobenzofuran-1,3-dione
CAS Number:
27550-59-0
Molecular Formula:
C8H4O4
Molecular Weight:
164.1150
MDL Number:
MFCD00997252
SMILES:
Oc1ccc2c(c1)C(=O)OC2=O
Properties
Properties
 
BP:
407.8±28.0°C at 760 mmHg  
Form:
Solid  
MP:
171-173°C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
235  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,1987,vol.30,#10,p.1798-1806

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,#20,p.4427-4431

[2]JournalofMedicinalChemistry,2011,vol.54,#1,p.342-353

[3]Patent:CN104910113,2017,B,.Locationinpatent:Page/Pagecolumn0041;0044-0046

[4]EuropeanJournalofMedicinalChemistry,1987,vol.22,p.229-238

[5]Patent:US2013/102576,2013,A1,.Locationinpatent:Paragraph0607

[6]Patent:WO2013/57013,2013,A2,.Locationinpatent:Page/Pagecolumn193

[7]Patent:US2013/90404,2013,A1,.Locationinpatent:Paragraph0075;0076;0077;0078

[8]Patent:US9393181,2016,B2,.Locationinpatent:Page/Pagecolumn9

[9]MonatsheftefuerChemie,1902,vol.23,p.401

[10]JournaloftheChemicalSociety,1907,vol.91,p.103

[11]ChemischeBerichte,1877,vol.10,p.1079

[12]JournalofMedicinalChemistry,1987,vol.30,#10,p.1798-1806

[13]JournaloftheChemicalSociety.PerkinTransactions2,1998,#5,p.1249-1256

[14]BioorganicandMedicinalChemistryLetters,2004,vol.14,#1,p.283-287

[15]Patent:EP1681283,2006,A1,.Locationinpatent:Page/Pagecolumn4-5

[16]Synthesis,2008,#21,p.3415-3422

[17]BioorganicandMedicinalChemistry,2010,vol.18,#14,p.5323-5338

[18]RSCAdvances,2015,vol.5,#96,p.79207-79215

[19]MarineDrugs,2016,vol.14,#6,

[1]RSCAdvances,2015,vol.5,#96,p.79207-79215

[2]Patent:CN104910113,2017,B,

[1]RSCAdvances,2015,vol.5,#96,p.79207-79215

[1]Patent:US2013/90404,2013,A1,

Downstream Synthesis Route

[1]RecueildesTravauxChimiquesdesPays-Bas,1949,vol.68,p.261,264

[1]Patent:US2874156,1955,

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4427-4431

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4427-4431

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4427-4431

Literature

Title: Synthesis and antimicrobial activity of N-analogous corollosporines.

Journal: Organic & biomolecular chemistry 20060407

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SDS
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