Substance
ID:177201
Names and Identifiers
IUPAC Traditional name
7-hydroxyflavone
IUPAC name
7-hydroxy-2-phenyl-4H-chromen-4-one
Synonyms
NSC 942587-羟基黄酮7-Hydroxyflavone7-Hydroxy-2-phenyl-4H-1-benzopyran-4-one
Properties
Product Information
Purity
≥98%
Safety Information
German water hazard class
3
Risk Statements
36/37/38
Safety Statements
26-37/39
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Precautionary statements
P261-P305+P351+P338
GHS Hazard statements
H315-H319-H335
GHS Signal Word
Warning
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
European Hazard Symbols
Irritant (Xi)Pharmacology Properties
Gene Information
mouse ... Hexa(15211)rat ... Ar(24208), Gabra2(29706)
Physical Property
Melting Point
245-247 °C(lit.)
Molecule Details
包装
1 g in poly bottle
Application
Reactant:
• Acting as a biologically valuable acceptor in O-glycosidation reactions1
• Involved in synthesis of fully phosphorylated flavones for use as pancreatic cholesterol esterase inhibitors2
• For O-methylation with di-Me carbonate3
• Linked by a polymethylene chain for synthesis of α1-adrenoceptor antagonists4
• Involved in Baylis-Hillman reactions5
• Involved in phase-transfer catalyzed glucosylation for synthesis of glucosylated flavonoids6
1 g in poly bottle
Application
Reactant:
• Acting as a biologically valuable acceptor in O-glycosidation reactions1
• Involved in synthesis of fully phosphorylated flavones for use as pancreatic cholesterol esterase inhibitors2
• For O-methylation with di-Me carbonate3
• Linked by a polymethylene chain for synthesis of α1-adrenoceptor antagonists4
• Involved in Baylis-Hillman reactions5
• Involved in phase-transfer catalyzed glucosylation for synthesis of glucosylated flavonoids6
Molecular Spectra
No Data Available
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References
No Data Available
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