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

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$16.00	$11.00
25g	98%	in stock	$58.00	$41.00
100g	98%	in stock	$91.00	$64.00

Description

• Catalog Number: AB67648
• 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

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

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

  Angewandte Chemie (International ed. in English) 20120427

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

  Cardiovascular research 20090301

• Stereochemical study of a novel tautomeric furanone, homofuraneol.

  Chirality 20090101

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

  Journal of cosmetic science 20080101

• 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.

  Bioscience, biotechnology, and biochemistry 20070701

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

  Journal of agricultural and food chemistry 20030226

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

  Chemical research in toxicology 20030101

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

  Microbiology (Reading, England) 20020401

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

  Journal of agricultural and food chemistry 20010201