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3-Methylthiophene CAS 616-44-4 EINECS NO 210-482-6

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Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 616-44-4

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3-Methylthiophene CAS 616-44-4

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CAS 616-44-4

CAS NO::
616-44-4
Appearance::
Light Brown Or Colorle Liquid
Molecular Formula::
C5H6S
Molecular Weight::
98.166100
EINECS NO::
210-482-6
MDL NO::
MFCD00005470
CAS NO::
616-44-4
Appearance::
Light Brown Or Colorle Liquid
Molecular Formula::
C5H6S
Molecular Weight::
98.166100
EINECS NO::
210-482-6
MDL NO::
MFCD00005470
3-Methylthiophene CAS 616-44-4 EINECS NO 210-482-6

Product Description:

Product Name: 3-Methylthiophene CAS NO: 616-44-4

 

 

Synonyms:

4-Methyl-3-thiopheneboronic acid;

Methylthiophene;

4-methylthiophene;

 

 

Chemical & Physical Properties:

Appearance: Light brown or colorle liquid

Assay :≥99.0%

Density: 1.016

Boiling Point: 115-117℃

Melting Point: -69℃

Flash Point: 11℃

Refractive Index: 1.518-1.52

Water Solubility: Insoluble

Stability: Stable under normal temperatures and pressures.

Storage Condition: Flammables area

Vapor Pressure: 42.4 mm Hg ( 37.7℃ )

 

 

Safety Information:

RTECS: XM9800000

Hazard Class: 3

Safety Statements: S16-S26-S37/39

HS Code: 29349990

WGK Germany: 3

Packing Group: II

RIDADR: UN 1993

Risk Statements: R11; R20/22; R36/37/38

Hazard Code: F

 

 

A thiophene derivative used as an electropolymerization monomer in conducting polymer research. Thiophene, 2-methyIthiopheney and 3-methylthiophene act as inhibitors for the polymerization of trichloroethylene in a solvent used for the degreasing of iron and aluminum, said polymerization being catalyzed by contact of the solvent with the metals. Bonz, in 1885, reported the formation of a dichloroethylthiophene from chlorination of 2-ethylthiophene in the cold. Is Opolski studied the chlorination of 2- and 3-methylthiophenes, 2-ethyl- and 2-butylthiophene and reported constants for the monochloro derivatives. Voerman has chlorinated 3-methylthiophene in the side chain with phosphorus trichloride in the sunlight, but concurrent ring chlorination predominates. 3-Methylthiophene gives a unique reaction with alkyl- or arylsodium in which the substitution takes place exclusively in the 5-position rather than in the expected 2-position.

 

 

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