| Weight | 177.066 g/mol |
|---|---|
| Formula | C5H5BrS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Bromo-3-methylthiophene (14282-76-9)
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- Selective direct arylation of 3-bromo-2-methylthiophene: a building-block for electro- and photoactive organic materials (Tetrahedron Letters, 2013)
- Thiophene series. Note IX . The absence of secondary steric effects in nucleophilic substitutions of thiophene derivatives: Kinetics of the reactions of 2-bromo-3,5-dinitrothiophene and 2-bromo-3,5-dinitro-4-methylthiophene with piperidine (Journal of Heterocyclic Chemistry, 1968)
- Multivariate Optimization and Mechanistic Considerations of the Amine Induced Ring-Opening Reaction of 2-Alkyl-3-bromo-5-methylthiophene-1,1-dioxides (Tetrahedron, 1998)
- A Versatile Organozinc Approach to the Synthesis of Potential Organic Functional Building Blocks: 5-Substituted 3-Bromo-2-Methylthiophene Derivatives (Bulletin of The Korean Chemical Society, 2015)
- ChemInform Abstract: Selective Direct Arylation of 3-Bromo-2-methylthiophene: A Building-Block for Electro- and Photoactive Organic Materials. (ChemInform, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C(SC=C1)Br
-
InChIKeyYYJBWYBULYUKMR-UHFFFAOYSA-N
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