38210-35-4

Basic information

• Product Name: 2-(2-PYRIDYL)BENZOTHIOPHENE, 97
• Synonyms: 2-(2-PYRIDYL)BENZOTHIOPHENE, 97;2-(2-Pyridyl)benzothiophene;2-(1-benzothiophen-2-yl)Pyridine;2-(2-Pyridyl)benzo[b]thiophene;2-(2-Pyridyl)benzothiophene 97%;Pyridine, 2-benzo[b]thien-2-yl-
• CAS NO: 38210-35-4
• Molecular Formula: C₁₃H₉NS
• Molecular Weight: 211.287
• EINECS: 200-258-5
• Mol File: 38210-35-4.mol
• Article Data: 32

Chemical Properties

• Melting Point: 123-127 °C
• Boiling Point: 380.659 °C at 760 mmHg
• Flash Point: 179.373 °C
• Appearance: /
• Density: 1.232 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.685
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Solubility: soluble in Toluene
• PKA: 3.80±0.19(Predicted)
• CAS DataBase Reference: 2-(2-PYRIDYL)BENZOTHIOPHENE, 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-PYRIDYL)BENZOTHIOPHENE, 97(38210-35-4)
• EPA Substance Registry System: 2-(2-PYRIDYL)BENZOTHIOPHENE, 97(38210-35-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 38210-35-4(Hazardous Substances Data)

Usage

General Description

2-(2-Pyridyl)benzothiophene, 97 is a chemical compound with the molecular formula C13H9NS. It is a heterocyclic aromatic compound that contains a benzothiophene ring with a pyridine group attached to the 2-position. 2-(2-PYRIDYL)BENZOTHIOPHENE, 97 is often used in organic synthesis and pharmaceutical research as a building block for creating a variety of different compounds. It is known to have a purity level of 97%, making it suitable for use in various laboratory and research applications. This chemical is not known to be hazardous to human health or the environment when handled and used according to proper safety guidelines.

InChI:InChI=1/C13H9NS/c1-2-7-12-10(5-1)9-13(15-12)11-6-3-4-8-14-11/h1-9H

Upstream product

• 109-04-6 2-bromo-pyridine 
• 98437-23-1 benzo[b]thiophene-2-boronic acid 
• 756480-40-7 benzo[b]thiophene-2-boric acid 
• 109-09-1 2-chloropyridine 
• 95-15-8 Benzo[b]thiophene 
• 142-08-5 2-hydroxypyridin 
• 1119275-23-8 1-iodo-2-((2-pyridinyl)ethynyl)benzene 
• 1945-84-2 2-ethynylpyridine 
• 615-42-9 1,2-Diiodobenzene 
• 583-53-9 2,3-dibromobenzene 
• 1209496-06-9 C₁₃H₁₅BO₃S 
• 568572-21-4 2-(benzo[b]thiophen-2-yl)boronic acid neopentyl glycol ester 
• 376584-76-8 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophene 
• 33775-94-9 2-(methylthio)iodobenzene 

Downstream Products

• 1232366-71-0 C₃₁H₃₀BNS 
• 1610885-82-9 (4-methoxyphenyl)(2-(pyridin-2-yl)benzo[b]thiophen-3-yl)methanone 
• 1610885-83-0 (4-Fluorophenyl)(2-(pyridin-2-yl)benzo[b]thiophen-3-yl)methanone 
• 1610885-81-8 (3,5-dimethylphenyl)(2-(pyridin-2-yl)benzo[b]thiophen-3-yl)methanone 
• 1627500-40-6 C₂₂H₁₂F₅NOS 

Relevant articles and documents

Synthesis of Bis-heteroaryls Using Grignard Reagents and Pyridylsulfonium Salts

Herein are reported ligand-coupling reactions of Grignard reagents with pyridylsulfonium salts. The method has wide functional group tolerance and enables the formation of bis-heterocycle linkages, including 2,4′-, 2,3′-, and 2,2′-bipyridines, as well as pyridines linked to pyrimidines, pyrazines, isoxazoles, and benzothiophenes. The methodology was successfully applied to the synthesis of the natural products caerulomycin A and E.

Trithiocarbonate Anion as a Sulfur Source for the Synthesis of 2,5-Disubstituted Thiophenes and 2-Substituted Benzo[ b]thiophenes

The trithiocarbonate anion (CS32-) was generated in situ from CS2 and KOH in dimethyl sulfoxide by a simple method and used as a novel synthetic equivalent of the S2- synthon for the synthesis of 2,5-disubstituted thiophenes from 1,3-butadiynes. Additionally, this system was employed for the metal-free synthesis of 2-substituted benzo[b]thiophenes from 2-haloalkynyl (hetero)arenes. These compounds were obtained from a cheap and readily available sulfur source in moderate to good yields, with good functional group tolerance.

The synthesis of cyclometalated platinum(ii) complexes with benzoaryl-pyridines as C^N ligands for investigating their photophysical, electrochemical and electroluminescent properties

A series of (C^N)Pt(acac)-type complexes has been successfully synthesized with a benzo[b]furan, benzo[b]thiophene, benzo[b]selenophene, or benzo[b]tellurophene group in the benzoaryl-pyridine ligand. Using X-ray crystallography, the chemical structures o