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7-hydroxy-2-methyl-4H-chromen-4-one

CAS No.
6320-42-9
Chemical Name:
7-hydroxy-2-methyl-4H-chromen-4-one
Synonyms
NSC 31894;Hymecromone EP Impurity B;7-Hydroxy-2-methylchromone;7-hydroxy-2-methylchromen-4-one;7-Hydroxy-2-methyl-4H-1-benzopyran-;7-hydroxy-2-methyl-1-benzopyran-4-one;7-Hydroxy-2-Methyl-4H-1-benzopyran-4-one;4H-1-Benzopyran-4-one, 7-hydroxy-2-Methyl-;Hymecromone Impurity 2 (Hymecromone EP Impurity B)
CBNumber:
CB62490146
Molecular Formula:
C10H8O3
Molecular Weight:
176.17
MDL Number:
MFCD00208225
MOL File:
6320-42-9.mol
MSDS File:
SDS
Last updated:2024-08-07 15:31:13

7-hydroxy-2-methyl-4H-chromen-4-one Properties

Melting point 254-255℃
Boiling point 345.5±42.0 °C(Predicted)
Density 1.319±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka 7.07±0.40(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319
Precautionary statements  P261-P305+P351+P338

7-hydroxy-2-methyl-4H-chromen-4-one price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000013 Hymecromone impurity B European Pharmacopoeia (EP) Reference Standard 6320-42-9 y0000013 $161 2024-03-01 Buy
TRC H947035 7-Hydroxy-2-methyl-4H-chromen-4-one 6320-42-9 100mg $105 2021-12-16 Buy
AK Scientific 2754BB 7-Hydroxy-2-methyl-4H-chromen-4-one 6320-42-9 1g $763 2021-12-16 Buy
American Custom Chemicals Corporation CHM0165657 7-HYDROXY-2-METHYL-4H-CHROMEN-4-ONE 95.00% 6320-42-9 1G $1351.35 2021-12-16 Buy
American Custom Chemicals Corporation CHM0165657 7-HYDROXY-2-METHYL-4H-CHROMEN-4-ONE 95.00% 6320-42-9 5G $2691.15 2021-12-16 Buy
Product number Packaging Price Buy
Y0000013 y0000013 $161 Buy
H947035 100mg $105 Buy
2754BB 1g $763 Buy
CHM0165657 1G $1351.35 Buy
CHM0165657 5G $2691.15 Buy

7-hydroxy-2-methyl-4H-chromen-4-one Chemical Properties,Uses,Production

Uses

7-Hydroxy-2-methyl-4H-chromen-4-one is used in the synthesis of 2,2-Dimethyl-2H-pyranoflavonol and pyranochromone derivatives.

Synthesis

Step(i): 7-Acetoxy-3-acetyl-2-methylchromone β-Resacetophenone (4.A.6) (10 g,0.066 mole) is heated with fusedsodium acetate (20 g) in acetic anhydride (30 ml) for 5 hr at 170-180°(oil bath) under anhydrous conditions. The reaction mixture is pouredover crushed ice, stirred well and left overnight.The separated product isfiltered and washed with water. It is crystallised from alcohol as light yellowneedles.Yield 10 g (58.5%).M.p.127° (lit. m.p.126-27°).
step (ii) : The above 7-acetoxy-3-acetyl-2-methylchromone (1 g,0.0038 mole) isrefluxed (2 hr) with aqueous sodium carbonate solution (10%,50 ml).Theclear solution is then acidified with hydrochloric acid (1:1).The separatedproduct is filtered and washed with water. It is crystallised from alcohol asthick prismatic crystals. Yield 0.5 g (73.5%).M.p. 249-50°.(lit. m.p.254-55°).
7-hydroxy-2-methyl-4H-chromen-4-one synthesis

7-hydroxy-2-methyl-4H-chromen-4-one Preparation Products And Raw materials

Raw materials

Preparation Products

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ATK CHEMICAL COMPANY LIMITED
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Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833 info@sagechem.com China 10266 58
NSC 31894 7-Hydroxy-2-Methyl-4H-1-benzopyran-4-one 4H-1-Benzopyran-4-one, 7-hydroxy-2-Methyl- 7-Hydroxy-2-methylchromone 7-hydroxy-2-methylchromen-4-one Hymecromone Impurity 2 (Hymecromone EP Impurity B) Hymecromone EP Impurity B 7-Hydroxy-2-methyl-4H-1-benzopyran- 7-hydroxy-2-methyl-1-benzopyran-4-one 6320-42-9