Basic information Safety Supplier Related

6-Methoxy-4-chromanone

Basic information Safety Supplier Related

6-Methoxy-4-chromanone Basic information

Product Name:
6-Methoxy-4-chromanone
Synonyms:
  • 6-Methoxy-4-chromanone
  • 6-methoxychroman-4-one
  • 4H-1-Benzopyran-4-one, 2,3-dihydro-6-Methoxy-
  • 2,3-Dihydro-6-methoxy-4H-benzopyran-4-one
  • 4-Chromanone, 6-methoxy-
  • 2,3-Dihydro-6-methoxychromen-4-one
  • JR-14070, 2,3-Dihydro-6-methoxychromen-4-one, 97%
  • 2,3-Dihydro-6-methoxy-4H-1-benzopyran-4-one
CAS:
5802-17-5
MF:
C10H10O3
MW:
178.18
Mol File:
5802-17-5.mol
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6-Methoxy-4-chromanone Chemical Properties

Melting point:
48 °C
Boiling point:
178-180 °C(Press: 23 Torr)
Density 
1.205
storage temp. 
Sealed in dry,Room Temperature
form 
powder to lump
color 
Light yellow to Yellow to Orange
InChI
InChI=1S/C10H10O3/c1-12-7-2-3-10-8(6-7)9(11)4-5-13-10/h2-3,6H,4-5H2,1H3
InChIKey
LQIYOSKKKUPTRP-UHFFFAOYSA-N
SMILES
C1OC2=CC=C(OC)C=C2C(=O)C1
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Safety Information

Risk Statements 
43
Safety Statements 
36/37
HS Code 
2932990090
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6-Methoxy-4-chromanone Usage And Synthesis

Synthesis

92971-94-3

5802-17-5

Representative procedure: synthesis of 6-methoxybenzodihydropyran-4-one (7a). 2,3-Dihydro-4H-chromen-4-one (1.20 g, 6.18 mmol) was dissolved in a mixed acetonitrile-water solvent (10 mL, V/V=1:2) followed by the addition of cerium ammonium nitrate (CAN, 5 g, 9.27 mmol). The reaction mixture was heated to 70 °C under stirring, maintained for 30 min and then cooled to room temperature. After completion of the reaction, the mixture was diluted with water and extracted with ether (3 x 20 mL). The organic phases were combined, washed with saturated sodium bicarbonate solution (20 mL), and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford the title compound 6-methoxybenzodihydropyran-4-one as a yellow oil (0.64 g, 70% yield).

References

[1] Tetrahedron Letters, 2012, vol. 53, # 33, p. 4280 - 4282

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