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2052-15-5,MFCD00009449
Catalog No.:AA0029V3

2052-15-5 | Pentanoic acid, 4-oxo-, butyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100g
98%+;RG
2 weeks  
$58.00   $41.00
- +
500g
98%+;RG
2 weeks  
$113.00   $79.00
- +
  • 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:
AA0029V3
Chemical Name:
Pentanoic acid, 4-oxo-, butyl ester
CAS Number:
2052-15-5
Molecular Formula:
C9H16O3
Molecular Weight:
172.2215
MDL Number:
MFCD00009449
SMILES:
CCCCOC(=O)CCC(=O)C
NSC Number:
78451
FEMA Number:
2207
Properties
Properties
 
BP:
240.3°C at 760 mmHg  
Refractive Index:
n20/D 1.427(lit.)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
152  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
1  

Upstream Synthesis Route

[1]Patent:CN103539665,2016,B,.Locationinpatent:Paragraph0063-0066

Downstream Synthesis Route

[1]CatalysisCommunications,2019,vol.123,p.109-113

[2]ChemSusChem,2011,vol.4,p.112-118

[3]GreenChemistry,2014,vol.16,p.1436-1443

[4]ChemCatChem,2014,vol.6,p.3080-3083

[5]RSCAdvances,2016,vol.6,p.22174-22178

[6]Molecularcatalysis,2020,vol.488

[7]RSCAdvances,2016,vol.6,p.90232-90238

[8]Patent:WO2018/112779,2018,A1.Locationinpatent:Page/Pagecolumn11

[9]Patent:WO2010/102203,2010,A2.Locationinpatent:Page/Pagecolumn24-25

[10]GreenChemistry,2013,vol.15,p.3367-3376

[11]CatalysisLetters,2018,vol.148,p.1731-1738

[12]Patent:US2763665,1952,

[13]Patent:US2763665,1952,

[14]NewJournalofChemistry,2019,vol.43,p.14694-14700

[1]Catalysisscienceandtechnology,2015,vol.5,p.5168-5173

[2]Catalysisscienceandtechnology,2015,vol.5,p.5168-5173

[3]Patent:US2493676,1947,

[1]JournaloftheAmericanChemicalSociety,1955,vol.77,p.3080

[1]Patent:US2406504,1944,

[1]BulletinoftheChemicalSocietyofJapan,1955,vol.28,p.54,56

Literature

Title: Conversion of biomass-derived levulinate and formate esters into γ-valerolactone over supported gold catalysts.

Journal: ChemSusChem 20111216

Title: Efficient conversion of furfuryl alcohol into alkyl levulinates catalyzed by an organic-inorganic hybrid solid acid catalyst.

Journal: ChemSusChem 20110117

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SDS
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Tags:2052-15-5 Molecular Formula|2052-15-5 MDL|2052-15-5 SMILES|2052-15-5 Pentanoic acid, 4-oxo-, butyl ester |Organic_Building_Blocks