Home Other Building Blocks 19322-27-1
19322-27-1,MFCD02752619
Catalog No.:AA003LFO

19322-27-1 | 4-Hydroxy-5-methyl-3-furanone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$17.00   $12.00
- +
25g
98%
in stock  
$62.00   $44.00
- +
100g
98%
in stock  
$97.00   $68.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003LFO
Chemical Name:
4-Hydroxy-5-methyl-3-furanone
CAS Number:
19322-27-1
Molecular Formula:
C5H6O3
Molecular Weight:
114.0993
MDL Number:
MFCD02752619
SMILES:
O=C1COC(=C1O)C
FEMA Number:
3635
Properties
Properties
 
BP:
218.3°C at 760 mmHg  
Form:
Solid  
MP:
129-133 °C(lit.)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
157  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.3  

Literature

Title: An efficient flow-photochemical synthesis of 5H-furanones leads to an understanding of torquoselectivity in cyclobutenone rearrangements.

Journal: Angewandte Chemie (International ed. in English) 20120427

Title: Norfuraneol dephosphorylates eNOS at threonine 495 and enhances eNOS activity in human endothelial cells.

Journal: Cardiovascular research 20090301

Title: Stereochemical study of a novel tautomeric furanone, homofuraneol.

Journal: Chirality 20090101

Title: A dual mechanism of 4-hydroxy-5-methyl-3[2H]-furanone inhibiting cellular melanogenesis.

Journal: Journal of cosmetic science 20080101

Title: Effects of the amino-carbonyl reaction of ribose and glycine on the formation of the 2(or 5)-ethyl-5(or 2)-methyl-4-hydroxy-3(2H)-furanone aroma component specific to miso by halo-tolerant yeast.

Journal: Bioscience, biotechnology, and biochemistry 20070701

Title: Formation of 5-methyl-4-hydroxy-3[2H]-furanone in cytosolic extracts obtained from Zygosaccharomyces rouxii.

Journal: Journal of agricultural and food chemistry 20030226

Title: Maillard reaction products modulating the growth of human tumor cells in vitro.

Journal: Chemical research in toxicology 20030101

Title: LuxS: its role in central metabolism and the in vitro synthesis of 4-hydroxy-5-methyl-3(2H)-furanone.

Journal: Microbiology (Reading, England) 20020401

Title: Heterocyclic volatiles formed by heating cysteine or hydrogen sulfide with 4-hydroxy-5-methyl-3(2H)-furanone at pH 6.5.

Journal: Journal of agricultural and food chemistry 20010201

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