2442-31-1 | 8-Hydroxy-2H-1-benzopyran-2-one

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$110.00	$77.00
250mg	98%	in stock	$249.00	$174.00
1g	98%	in stock	$646.00	$452.00
5g	98%	in stock	$2,245.00	$1,571.00

Description

• Catalog Number: AF52541
• Chemical Name: 8-Hydroxy-2H-1-benzopyran-2-one
• CAS Number: 2442-31-1
• Molecular Formula: C9H6O3
• Molecular Weight: 162.14214
• MDL Number: MFCD18450722
• SMILES: O=c1ccc2c(o1)c(O)ccc2

Computed Properties

• Complexity: 222
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.6

Literature

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  Biochemistry and cell biology = Biochimie et biologie cellulaire 20121001

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  Bioresource technology 20120301

• F420H2-dependent degradation of aflatoxin and other furanocoumarins is widespread throughout the actinomycetales.

  PloS one 20120101

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  Bioresource technology 20101001

• Quinoline biodegradation and its nitrogen transformation pathway by a Pseudomonas sp. strain.

  Biodegradation 20100601

• Cysteine as a modulator residue in the active site of xenobiotic reductase A: a structural, thermodynamic and kinetic study.

  Journal of molecular biology 20100423

• Interaction of 8-hydroxyquinoline with soil environment mediates its ecological function.

  PloS one 20100101

• Kinetic characterization of xenobiotic reductase A from Pseudomonas putida 86.

  Biochemistry 20091208

• Aerobic biodegradation characteristics and metabolic products of quinoline by a Pseudomonas strain.

  Bioresource technology 20091101

• Synthesis of hydroxycoumarins and hydroxybenzo[f]- or [h]coumarins as lipid peroxidation inhibitors.

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  Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20090201

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  Huan jing ke xue= Huanjing kexue 20081201

• Xenobiotic reductase A in the degradation of quinoline by Pseudomonas putida 86: physiological function, structure and mechanism of 8-hydroxycoumarin reduction.

  Journal of molecular biology 20060804

• Coumarin metabolism by rat esophageal microsomes and cytochrome P450 2A3.

  Chemical research in toxicology 20011001