13781-37-8

Basic information

• Product Name: 2-iodo-5-phenylthiophene
• Synonyms: 2-iodo-5-phenylthiophene;Thiophene, 2-iodo-5-phenyl- (Related Reference)
• CAS NO: 13781-37-8
• Molecular Formula: C₁₀H₇IS
• Molecular Weight: 286.13205
• Mol File: 13781-37-8.mol
• Article Data: 7

Chemical Properties

• Melting Point: 82.0 to 86.0 °C
• Boiling Point: 329.1±30.0 °C(Predicted)
• Appearance: /
• Density: 1.720±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-iodo-5-phenylthiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodo-5-phenylthiophene(13781-37-8)
• EPA Substance Registry System: 2-iodo-5-phenylthiophene(13781-37-8)

Safety Data

• Hazardous Substances Data: 13781-37-8(Hazardous Substances Data)

Usage

General Description

2-iodo-5-phenylthiophene is a chemical compound with the molecular formula C10H7IS. It is a member of the thiophene family, which are heterocyclic compounds containing a five-membered ring with four carbon atoms and one sulfur atom. The presence of both iodine and a phenyl group in its structure makes 2-iodo-5-phenylthiophene a valuable building block for the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in organic synthesis and materials science due to its unique properties and reactivity. Additionally, its potential as a ligand in transition metal-catalyzed cross-coupling reactions has garnered interest in the field of organic chemistry.

Upstream product

• 825-55-8 2-phenylthiophene 
• 7553-56-2 iodine 
• 71-43-2 benzene 
• 98-80-6 phenylboronic acid 
• 108-86-1 bromobenzene 

Downstream Products

• 83495-30-1 5,5′-diphenyl-2,2′-bithiophene 
• 1665-32-3 5,5-diphenyl-2,2':5',2-terthiophene 
• 641609-90-7 C₃₅H₂₂F₆S₄ 
• 641609-91-8 C₃₉H₃₀F₆S₄ 
• 1204-82-6 2-Phenyl-5-(1'-propynyl)-thiophene 
• 62404-17-5 N-(5-phenyl-2-thenoyl)piperidine 
• 17361-89-6 5-phenyl-2-thiophene carbonyl chloride 
• 96924-61-7 (Z)-3-chloro-2-methyl-(5-phenyl-2-thienyl)acrolein 
• 96924-60-6 (E)-3-chloro-2-methyl-3-(5-phenyl-2-thienyl)acrolein 
• 94742-70-8 2-phenyl-5-(3-buten-1-ynyl)thiophen 
• 1665-35-6 5-ethynyl-2-phenylthiophene 
• 256342-39-9 1,4-bis(5-phenylthiophene-2-yl)benzene 
• 19163-24-7 5-phenyl-2-thiophenecarboxylic acid 
• 1665-31-2 5-phenyl-[2,2'-bithienyl] 

Relevant articles and documents

Synthesis of thiophene/phenylene co-oligomers. I. Phenyl-capped oligothiophenes

We report the synthesis of phenyl-capped oligothiophenes via improved synthetic schemes. These schemes are based on the Grignard coupling reaction and enable us to obtain the target compounds at high yields. The resulting materials have been fully charact

Disulfide-Catalyzed Iodination of Electron-Rich Aromatic Compounds

Herein, a disulfide-catalyzed electrophilic iodination of aromatic compounds using 1,3-diiodo-5,5-dimethylhydantoin (DIH) has been developed. The disulfide activates DIH as a Lewis base to promote the iodination reaction in acetonitrile under mild conditions. This system is applicable to a wide range of electron-rich aromatic compounds, including acetanilide, anisole, imidazole, and pyrazole derivatives.

Light-controlled reversible modulation of frontier molecular orbital energy levels in trifluoromethylated diarylethenes

Among bistable photochromic molecules, diarylethenes (DAEs) possess the distinct feature that upon photoisomerization they undergo a large modulation of their pelectronic system, accompanied by a marked shift of the HOMO/LUMO energies and hence oxidation/