38071-58-8

Basic information

• Product Name: 4-BROMO-2-PHENYLTHIOPHENE
• Synonyms: 4-BROMO-2-PHENYLTHIOPHENE
• CAS NO: 38071-58-8
• Molecular Formula: C₁₀H₇BrS
• Molecular Weight: 239.13
• Mol File: 38071-58-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-BROMO-2-PHENYLTHIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2-PHENYLTHIOPHENE(38071-58-8)
• EPA Substance Registry System: 4-BROMO-2-PHENYLTHIOPHENE(38071-58-8)

Safety Data

• Hazardous Substances Data: 38071-58-8(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 3140-92-9 2,4-dibromothiophene 
• 98-80-6 phenylboronic acid 
• 108-94-1 cyclohexanone 
• 38071-57-7 4-bromo-2-(1-cyclohexenyl)thiophene 

Downstream Products

• 1127611-03-3 2-phenyl-4-(trans-styryl)thiophene 
• 223675-40-9 4-(2'-methoxyphenyl)-2-phenylthiophene 
• 825-55-8 2-phenylthiophene 
• 38115-12-7 5-phenylthiophene-3-carboxaldehyde 
• 1520923-54-9 2,5,8,11-tetraphenylcycloocta[1,2-b:4,3-b':5,6-b'':8,7-b''']tetrathiophene 
• 83495-28-7 5,5’-diphenyl-3,3’-bithiophene 
• 937281-16-8 5-phenyl-3-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)thiophene 
• 362612-67-7 2-phenyl-4-thiopheneboronic acid 

Relevant articles and documents

Composite tetraheteroarylenes and related higher cyclic oligomers of heteroarenes produced by palladium-catalyzed direct coupling

Substantial research interests have been focused on cyclic π-conjugated molecules owing to their unique chemical and physical properties. By constructing hybrid aromatic arrays within these cyclic systems, new series of composite macrocycles would be prov

METABOTROPIC GLUTAMATE RECEPTOR NEGATIVE ALLOSTERIC MODULATORS (NAMS) AND USES THEREOF

Provided herein are small molecule active metabotropic glutamate subtype-2 and -3 receptor negative allosteric modulators (NAMs), compositions comprising the compounds, and methods of using the compounds and compositions.

Room-temperature hydrodehalogenation of halogenated heteropentalenes with one or two heteroatoms

The pair NaBH4-TMEDA as a hydride source and catalytic PdCl 2(dppf) in THF prove to be an efficient system for the hydrodehalogenation of bromo(chloro)-heteropentalenes with one or two heteroatoms, while Pd(OAc)2/PPh3 is able to reduce reactive haloheteropentalenes, and PdCl2(tbpf) allows the removal of the 2-chlorine from a thiophene ring. The reaction conditions tolerate various functional groups, allowing highly chemoselective reactions in the presence of halide, ester, alkyne, alkene, and nitrile substituents and also showing good efficiency in the regioselective hydrodehalogenation of a variety of polyhalogenated substrates.