Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 616-44-4
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Plastic bottles, Plastic buckets
Delivery Time: 7-15 days
Payment Terms: L/C, D/A, T/T, Western Union
Supply Ability: TON
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 |
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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