3-Methylthiophene CAS 616-44-4
3-Methylthiophene , Promotion Season Now in Store and Free Sample for Testing with Factory Price
Chemical Name: 3-Methylthiophene
CAS No.: 616-44-4
Molecular Fomula: C5H6S
Molecular weight:98.17
Appearance: Clear colorless to light yellow Liquid
Sample: Available
3-Methylthiophene: The Complete Guide
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Description of 3-Methylthiophene
A thiophene derivative used as an electropolymerization monomer in conducting polymer research.
Basic Info of 3-Methylthiophene
Basic Info
Chemical Name | 3-Methylthiophene |
Synonyms | 3-methyl thiophene;4-Methyl-3-thienylboronic acid;4-Methyl-3-thiopheneboronic acid;Methylthiophene;3-methylthiene;Expand |
CAS No. | 616-44-4 |
Molecular Formula | C5H6S |
Molecular Weight | 98.16610 |
PSA | 28.24000 |
LogP | 2.05650 |
Safety Info
RTECS | XM9800000 |
Hazard Class | 3 |
Safety Statements | S16-S26-S37/39 |
HS Code | 29349990 |
Packing Group | II |
WGK Germany | 3 |
RIDADR | UN 1993 |
Risk Statements | R11; R20/22; R36/37/38 |
Hazard Codes | F |
Properties
Appearance & Physical State | light brown or colorle liquid |
Density | 1.016 |
Boiling Point | 115-117ºC |
Melting Point | -69ºC |
Flash Point | 11ºC |
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 °C) |
Numbering system
EINECS number | 210-482-6 |
MDL number | MFCD00005470 |
What is 3-Thiotolene?
- With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is 3-Methylthiophene which has developed particularly rapidly in recent years. Do you know about 3-Methylthiophene?
- The official answer:3-Methylthiophene is a chemical compound with the molecular formula C5H6S.
What’s the application of 3-Thiotolene?
Used as a reactant for the preparation of the herbicide thiophenone, as a starting reagent for the preparation of disulfide esters and as an intermediate for the synthesis of thiophenothiopyr, also for the preparation of homopolymers, dopants, photochromic materials, optical recording media and thermally stable photoresponsive materials.
Conclusion
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