872-31-1
872-31-1
Chemical Structure
3-Bromothiophene
- CAS No.: 872-31-1
- Formula:C4H3BrS
- Molecular Weight:163.04
IUPAC Name: 3-bromothiophene
InChIKey: XCMISAPCWHTVNG-UHFFFAOYSA-N
SMILES: BrC1=CSC=C1
Biological Activity: 3-Bromothiophene is a bromine atom-substituted 3-halogenated thiophene. Polymers of 3-Bromothiophene are conductive polymers and have potential optoelectronic application value. Additionally, 3-Bromothiophene serves as a key intermediate for the synthesis of a variety of important pharmaceuticals, agrochemicals, and cosmetics[1][2][3].
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3-Bromothiophene | 99.63% | 3-Bromothiophene is a bromine atom-substituted 3-halogenated thiophene. Polymers of 3-Bromothiophene are conductive polymers and have potential optoelectronic application value. Additionally, 3-Bromothiophene serves as a key intermediate for the synthesis of a variety of important pharmaceuticals, agrochemicals, and cosmetics. | ||||||||||||||||||||
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References
- [1]. Casanovas J, Aradilla D, Poater J, Solà M, Estrany F, Alemán C. Properties of poly(3-halidethiophene)s. Phys Chem Chem Phys. 2012 Jul 28;14(28):10050-62. [Content Brief]
- [2]. Gosmini C, Nédélec J Y, Périchon J. Electrosynthesis of 3-thienylzinc bromide from 3-bromothiophene via a nickel catalysis[J]. Tetrahedron letters, 1997, 38(11): 1941-1942.
- [3]. Ashalatha B V, et al. Synthesis and characterization of some novel 3-bromo-2-acetylthiophene chalcones and biological evaluation of their ethyl-4-(3-bromothien-2-yl)-2-oxo-6-(aryl) cyclohex-3-ene-1-carboxylate derivatives. Phosphorus, Sulfur, and Silicon, 2009, 184(7): 1904-1919.
Keywords
