6-METHYL-4-CHROMANONE Chemical Properties

Melting point:

31-35 °C (lit.)

Boiling point:

141-143 °C/13.5 mmHg (lit.)

Density 

1.071 g/mL at 25 °C (lit.)

refractive index 

1.5550

Flash point:

>230 °F

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

solubility 

soluble in Methanol

form 

powder to lump

color 

White to Almost white

Specific Gravity

1.071

CAS DataBase Reference

39513-75-2(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

2932990090

MSDS

• Language:English Provider:SigmaAldrich

6-METHYL-4-CHROMANONE Usage And Synthesis

Uses

The product has been used as a substrate for carbonyl reductase from Sporobolomyces salmonicolor, wherein it was reduced to the corresponding (R)-chiral alcohol. It has also been used as a substrate for the enantioselective reduction by 3 biocatalysts, namely, Didymosphaeria igniaria, Coryneum betulinum and Chaetomium sp.

Synthesis

Representative procedure: synthesis of 6-methylbenzodihydropyran-4-one (7a). To 2,3-dihydro-4H-chromen-4-one (4a, 1.20 g, 6.18 mmol) in an acetonitrile-water mixture (10 mL, 1:2, v/v) was added cerium ammonium nitrate (CAN, 5 g, 9.27 mmol). The reaction mixture was heated to 70 °C under stirring, maintained for 30 min and subsequently cooled to room temperature. The reaction mixture was diluted with water and extracted with ether (3 x 20 mL). The combined organic layers were washed with saturated sodium bicarbonate solution (20 mL) and subsequently dried over anhydrous magnesium sulfate. After filtration, the mixture was concentrated under reduced pressure to give 6-methylbenzodihydropyran-4-one as a yellow oil (0.64 g, 70% yield).

References

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

6-METHYL-4-CHROMANONE(39513-75-2)Related Product Information

• BAVACHININ A
• 6,8-DIMETHYL-4',5,7-TRIHYDROXYFLAVANONE
• GAMBOGIC ACID
• 6-METHYL-4-CHROMANONE
• 2'-hydroxymatteucinol
• 2-Butenal, 2-methyl-4-[3a,4,5,7-tetrahydro-8-hydroxy-3,3,11,11-tetramethyl-13-(3-methyl-2-butenyl)-7,15-dioxo-1,5-methano-1H,3H,11H-furo[3,4-g]pyrano[3,2-b]xanthen-1-yl]-, [1R-[1alpha,1(Z),3abeta,5alpha,14aS*]]-
• 6-FLUORO-2-METHYL-4-CHROMANONE,6-Fluoro-2-methyl-4-chromanone97%
• LUPINIFOLIN
• LUPINIFOLINOL
• Poriolide
• matteuorienate A
• 5,7-DIHYDROXY-6-METHYLFLAVANONE
• matteuorienate B
• 12-ALPHA-DEOXYTEPHROSIN
• 6,8-DIPRENYLNARINGENIN
• Isoporiolide
• 6-ETHYLCHROMAN-4-ONE
• 6-PRENYLNARINGENIN