Basic information Safety Supplier Related

6-METHYLBENZOTHIOPYRAN-4(4H)-ONE

Basic information Safety Supplier Related

6-METHYLBENZOTHIOPYRAN-4(4H)-ONE Basic information

Product Name:
6-METHYLBENZOTHIOPYRAN-4(4H)-ONE
Synonyms:
  • 6-METHYLBENZOTHIOPRAN-4(4H)-ONE
  • 6-METHYLBENZOTHIOPYRAN-4(4H)-ONE
  • 6-METHYLTHIOCHROMAN-4-ONE
  • 6-METHYLTHIOCHROMANONE
  • 2,3-dihydro-6-methyl-4H-1-benzothiopyran-4-one
  • 3,4-Dihydro-6-methyl-2H-1-benzothiopyran-4-one
  • Einecs 230-114-8
  • 6-methyl-4H-thiochromen-4-one
CAS:
6948-34-1
MF:
C10H10OS
MW:
178.25
EINECS:
230-114-8
Mol File:
6948-34-1.mol
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6-METHYLBENZOTHIOPYRAN-4(4H)-ONE Chemical Properties

Melting point:
41-45 °C(lit.)
Boiling point:
174 °C(Press: 10 Torr)
Density 
1.200±0.06 g/cm3(Predicted)
Flash point:
110 °C
storage temp. 
Sealed in dry,Room Temperature
Appearance
Light yellow to orange Solid
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
2934999090

MSDS

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6-METHYLBENZOTHIOPYRAN-4(4H)-ONE Usage And Synthesis

Synthesis

13739-35-0

6948-34-1

General procedure for the synthesis of 6-methylthiobenzodihydropyran-4-one from 3-[(4-methylphenyl)thio]propionic acid: 20 g (0.1 mol) of 3-[(4-methylphenyl)thio]propionic acid was dissolved in a 1000 ml beaker containing 70 ml of concentrated sulphuric acid, and the reaction was carried out for 12 h at room temperature. Upon completion of the reaction, the reaction mixture was cooled in an ice-water bath to precipitate a large amount of yellow solid precipitate, which was subsequently filtered. The filter cake was washed sequentially with 5% sodium bicarbonate solution and distilled water until neutral. The crude product was purified by recrystallization from 50% ethanol solution to give 16.88 g of light yellow solid 6-methylthiobenzodihydropyran-4-one in 93% yield.

References

[1] Letters in Organic Chemistry, 2016, vol. 13, # 3, p. 206 - 216
[2] Journal of Chemical Research, 2004, # 6, p. 394 - 395
[3] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 13, p. 4569 - 4574
[4] Chinese Journal of Chemistry, 2011, vol. 29, # 4, p. 757 - 764
[5] Chemische Berichte, 1923, vol. 56, p. 1275

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