4-hydroxy-2H-1-benzopyran-2-one

CAS: 3690-05-9 C9 H6 O3 MW: 162.14442000

Identification

Name4-hydroxy-2H-1-benzopyran-2-one
CAS Number3690-05-9
FDA UNII61POZ1QQ11
Molecular FormulaC9 H6 O3
Molecular Weight162.14442000
Nikkaji NumberJ117.130E

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 6.393e+004 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 4-hydroxy-2H-1-benzopyran-2-one usage levels up tonot for fragrance use.
Recommendation for 4-hydroxy-2H-1-benzopyran-2-one flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

p- coumaryl alcohol p- hydroxycinnamic alcohol 4-[(E)-3- hydroxyprop-1-enyl]phenol phenol, 4-(3-hydroxy-1-propenyl)- PubMed: Synthesis and insecticidal activity of new 4-hydroxy-2H-1-benzopyran-2-one derivatives. PubMed: Synthesis, spectroscopy and alkylating properties of Pd(II) complexes of phosphorohydrazones of coumarin and chromone with potential antibacterial activity. PubMed: Synthesis, characterization, and cytotoxic activity of new lanthanum(III) complexes of bis-coumarins. PubMed: Synthesis and anticoagulant activities of substituted 2,4-diketochromans, biscoumarins, and chromanocoumarins. PubMed: Synthesis, structure, toxicological and pharmacological investigations of 4-hydroxycoumarin derivatives. PubMed: Cytotoxic activity of new cerium (III) complexes of bis-coumarins. PubMed: Cytotoxic activity of new neodymium (III) complexes of bis-coumarins. PubMed: Synthesis and pharmacological investigations of some 4-hydroxycoumarin derivatives. PubMed: High pressure liquid chromatographic determination of the rodenticide brodifacoum in rat tissue.