2H-1-Benzopyran-2-one,4,7-dihydroxy-

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Names

[ CAS No. ]:
1983-81-9

[ Name ]:
2H-1-Benzopyran-2-one,4,7-dihydroxy-

[Synonym ]:
4,7-dihydroxy-2H-1-benzopyran-2-one
4,7-Dihydroxycoumarin
Coumarin,4,7-dihydroxy
4,7-dihydroxy-2H-chromen-2-one
4,7-Dihydroxy-cumarin
4,7-Dihydroxy-coumarin
4,7-dihydroxy-chromen-2-one
4,7-Dihydroxy-2-oxo-2H-1-benzopyran
2H-1-BENZOPYRAN-2-ONE,4,7-DIHYDROXY
2,7-dihydroxychromen-4-one

Chemical & Physical Properties

[ Density]:
1.612g/cm3

[ Boiling Point ]:
390ºC at 760mmHg

[ Melting Point ]:
263 °C(dec.)

[ Molecular Formula ]:
C9H6O4

[ Molecular Weight ]:
178.14200

[ Flash Point ]:
166.5ºC

[ Exact Mass ]:
178.02700

[ PSA ]:
70.67000

[ LogP ]:
1.20420

[ Vapour Pressure ]:
0mmHg at 25°C

[ Index of Refraction ]:
1.711

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2932209090

Synthetic Route

Customs

[ HS Code ]: 2932209090

[ Summary ]:
2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites.

Arch. Biochem. Biophys. 564 , 244-53, (2014)

The widely used anticoagulant Coumadin (R/S-warfarin) undergoes oxidation by cytochromes P450 into hydroxywarfarins that subsequently become conjugated for excretion in urine. Hydroxywarfarins may mod...


More Articles


Related Compounds

  • 2H-1-Benzopyran-2-one,4,7-dihydroxy-8-methyl
  • 2H-1-Benzopyran-2-one,4,7-dihydroxy-8-methoxy-5-methyl
  • 2H-1-Benzopyran-2-one,4,7-dihydroxy-3-methoxy-5-(2-propenyloxy)
  • 4,7-Dihydroxy-3-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-2H-1-benzopyran-2-one
  • (R)-7-Hydroxy Warfarin
  • (4bβ)-1-Methyl-2β,3α,7-trihydroxy-8-methylenegibba-4-ene-1α,10β-dicarboxylic acid 1,3-lactone
  • N~1~-(3-chlorobenzyl)-2-[3-(2-methoxyphenyl)-6-oxo-1(6H)-pyridazinyl]acetamide
  • 2-[5-(4-methoxyphenyl)-3-methyl-1H-pyrazol-4-yl]-N-[2-(1,3-thiazol-2-yl)ethyl]acetamide
  • N-(1,1-dioxidotetrahydrothiophen-3-yl)-1-methyl-1H-indole-4-carboxamide
  • 1-[4-(Methylsulfonyl)piperazino]-6-(2-pyrimidinylamino)-1-hexanone
  • N-[2-(5-chloro-1H-indol-3-yl)ethyl]-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxamide
  • 2'-cyclohexyl-N-cyclopropyl-1'-oxo-1',4'-dihydro-2'H-spiro[cyclohexane-1,3'-isoquinoline]-4'-carboxamide
  • 2,4-dichloro-N-[2-(2-methyl-4-oxopyrido[2,3-d]pyrimidin-3(4H)-yl)ethyl]benzamide
  • N-(1-methyl-1H-benzimidazol-5-yl)-1-(propan-2-yl)-1H-indole-4-carboxamide
  • 2-chloro-5-(propan-2-yl)-N-{[1-(propan-2-yl)-1H-benzimidazol-2-yl]methyl}-1,3-thiazole-4-carboxamide
  • 3-(4-chlorophenyl)-4-(1H-pyrrol-1-yl)-N-(3,4,5-trimethoxyphenyl)butanamide
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