Home Other Building Blocks 19444-84-9
19444-84-9,MFCD00134268
Catalog No.:AA00I2ZF

19444-84-9 | Alpha-hydroxy-gamma-butyrolactone

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250mg
95%
in stock  
$8.00   $6.00
- +
1g
95%
in stock  
$19.00   $14.00
- +
5g
95%
in stock  
$41.00   $29.00
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10g
95%
in stock  
$80.00   $56.00
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25g
95%
in stock  
$197.00   $138.00
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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:
AA00I2ZF
Chemical Name:
Alpha-hydroxy-gamma-butyrolactone
CAS Number:
19444-84-9
Molecular Formula:
C4H6O3
Molecular Weight:
102.0886
MDL Number:
MFCD00134268
SMILES:
O=C1OCCC1O
Properties
Computed Properties
 
Complexity:
88.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-0.4  

Upstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2015,vol.54,#17,p.5196-5200

[2]Angew.Chem.,2015,vol.127,#17,p.5285-5289,5

[1]DRP/DRBPOrg.Chem.,

[1]OrganicLetters,2013,vol.15,#6,p.1170-1173

[1]OrganicLetters,2013,vol.15,#6,p.1170-1173

[1]OrganicLetters,2013,vol.15,#24,p.6132-6135

Downstream Synthesis Route

[1]Patent:DE812551,1949,    DRP/DRBPOrg.Chem.,

[1]Brennan,John;Murphy,PatrickJ.[TetrahedronLetters,1988,vol.29,#17,p.2063-2066]

[2]CurrentPatentAssignee:EVONIKINDUSTRIESAG-US2009/318715,2009,A1Locationinpatent:Page/Pagecolumn4

[3]CurrentPatentAssignee:CHINESEACADEMYOFSCIENCES-CN112876394,2021,ALocationinpatent:Paragraph0008;0018-0019

[1]Ringdahl;Craig[ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1980,vol.34,#10B,p.731-733]

3970-21-6    19444-84-9   
2-methoxyethoxymethoxy-γ-butyrolactone 

[1]Tuck,KellieL.;Saldanha,S.Adrian;Birch,LouiseM.;Smith,AlisonG.;Abell,Chris[OrganicandBiomolecularChemistry,2006,vol.4,#19,p.3598-3610]

[2]Wuensch,Bernhard;Diekmann,Heike[Heterocycles,1994,vol.38,#4,p.709-712]

75-77-4    19444-84-9   
α-trimethylsilyloxy-γ-butyrolactone 

[1]Hopper,AllenT.;Witiak,DonaldT.;Ziemniak,John[JournalofMedicinalChemistry,1998,vol.41,#4,p.420-427]

Literature

Title: Isolation and properties of a levo-lactonase from Fusarium proliferatum ECU2002: a robust biocatalyst for production of chiral lactones.

Journal: Applied microbiology and biotechnology 20070701

Title: Negative electrospray, ion trap multistage mass spectrometry of synthetic fragments of the O-PS of Vibrio cholerae O:1.

Journal: European journal of mass spectrometry (Chichester, England) 20060101

Title: Positive-ion fragmentation in matrix-assisted laser desorption/ionization tandem time of flight mass spectrometry of synthetic analogs of the O-specific polysaccharide of Vibrio cholerae O:1.

Journal: European journal of mass spectrometry (Chichester, England) 20060101

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SDS
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