| Identification | Back Directory | [Name]
2-BROMO-5-PHENYLTHIOPHENE | [CAS]
29488-24-2 | [Synonyms]
2-BROMO-5-PHENYLTHIOPHENE
5-Bromo-2-phenylthiophene
2-Bromo-5-phenylthiophene, 95+% | [Molecular Formula]
C10H7BrS | [MDL Number]
MFCD00159575 | [MOL File]
29488-24-2.mol | [Molecular Weight]
239.13 |
| Chemical Properties | Back Directory | [Melting point ]
83 °C | [Boiling point ]
289℃ | [density ]
1.490 | [Fp ]
129℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
powder to crystal | [color ]
White to Light yellow | [InChI]
InChI=1S/C10H7BrS/c11-10-7-6-9(12-10)8-4-2-1-3-5-8/h1-7H | [InChIKey]
RVCTZBRMQZWVDA-UHFFFAOYSA-N | [SMILES]
C1(Br)SC(C2=CC=CC=C2)=CC=1 | [CAS DataBase Reference]
29488-24-2 |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2-bromo-5-phenylthiophene from 2-phenylthiophene: 2-phenylthiophene (1.5 g, 9.4 mmol) was completely dissolved in chloroform (100 mL), followed by slow addition of N-bromosuccinimide (1.7 g, 9.4 mmol). The reaction mixture was stirred at room temperature for 30 min. Upon completion of the reaction, the solvent was completely removed by distillation under reduced pressure. Subsequently, ethanol was added to the residue at 0 °C and stirred for 20 min. The resulting precipitate was collected by filtration and the filtrate was dried under vacuum at room temperature to afford 2-bromo-5-phenylthiophene (2.2 g) in 100% yield. | [References]
[1] Patent: WO2008/153338, 2008, A2. Location in patent: Page/Page column 30-31
[2] Chemistry - An Asian Journal, 2014, vol. 9, # 9, p. 2542 - 2547,6
[3] Tetrahedron Letters, 2004, vol. 45, # 38, p. 7157 - 7161
[4] New Journal of Chemistry, 2009, vol. 33, # 6, p. 1362 - 1367
[5] Tetrahedron, 1997, vol. 53, # 30, p. 10357 - 10400 |
|
|