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p-methylthioanisole

Names

[ CAS No. ]:
1879-16-9

[ Name ]:
p-methylthioanisole

[Synonym ]:
p-(Methylthio)anisole
4-Methoxy thioanisole
Benzene, 1-methoxy-4-(methylthio)-
4-(Methylthio)anisole
Anisole, p-(methylthio)-
1-Methoxy-4-methylthiobenzene
p-Methoxyphenyl methyl sulfide
Benzene, 1-methoxy-4- (methylthio)-
Anisole, p- (methylthio)-
1-Methoxy-4-(Methylthio)Benzene
MFCD00010587
4-OMe-phenyl methyl sulfide
1-Methoxy-4-(methylsulfanyl)benzene
p-methylthioanisole
Methyl 4-(methylsulfanyl)phenyl ether
Methyl 4-methoxyphenyl sulfide
Methyl p-methoxyphenyl sulfide
p-Anisyl methyl sulfide

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
253.4±0.0 °C at 760 mmHg

[ Melting Point ]:
22-23 °C

[ Molecular Formula ]:
C8H10OS

[ Molecular Weight ]:
154.229

[ Flash Point ]:
107.8±0.0 °C

[ Exact Mass ]:
154.045242

[ PSA ]:
34.53000

[ LogP ]:
3.08

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.554

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
UN 3335

[ HS Code ]:
2930909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Transient-state kinetics of the reactions of 1-methoxy-4-(methylthio)benzene with horseradish peroxidase compounds I and II.

Biochemistry 29(11) , 2757-63, (1990)

Transient-state reactions of horseradish peroxidase compounds I and II with 1-methoxy-4-(methylthio)benzene (a para-substituted thioanisole) were studied over the pH range from 3.4 to 10.5. The pH-jum...

Iron-catalyzed selective oxidation of sulfides to sulfoxides with the polyethylene glycol/O2 system. Li B, et al.

Green Chem. 14(1) , 130-35, (2012)


More Articles


Related Compounds

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