2-Picoline, 98+%
2-Picoline, 98+%
2-Picoline, 98+%
Thermo Scientific Chemicals

2-Picoline, 98+%

CAS: 109-06-8 | C6H7N | 93.129 g/mol
数量:
100 mL
500 mL
2500 mL
製品番号(カタログ番号) A10847.0F
または、製品番号A10847-0F
価格(JPY)
-
数量:
2500 mL
一括またはカスタム形式をリクエストする
化学物質識別子
CAS109-06-8
IUPAC Name2-methylpyridine
Molecular FormulaC6H7N
InChI KeyBSKHPKMHTQYZBB-UHFFFAOYSA-N
SMILESCC1=CC=CC=N1
さらに表示
FormLiquid
Appearance (Color)Clear, colorless to yellow
Assay from Supplier's CofA≥98.0%
2-Picoline is used as an intermediate in agrochemicals and pharmaceuticals. It serves as a solvent as well as to prepare dyes and resins. It finds application as a constituent in cigarette smoke, bone oil, coal tar and coke oven emissions. Further, it acts as a precursor of 2-vinylpyridine, picolinic acid and nitrapyrin. It is also employed to study the electron and proton transfer reactions of lumiflavin. In addition, it is used in the synthetic pathway for the preparation of dearomatized, allylated and carbon-hydrogen bond activated pyridine derivatives.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Picoline is used as an intermediate in agrochemicals and pharmaceuticals. It serves as a solvent as well as to prepare dyes and resins. It finds application as a constituent in cigarette smoke, bone oil, coal tar and coke oven emissions. Further, it acts as a precursor of 2-vinylpyridine, picolinic acid and nitrapyrin. It is also employed to study the electron and proton transfer reactions of lumiflavin. In addition, it is used in the synthetic pathway for the preparation of dearomatized, allylated and carbon-hydrogen bond activated pyridine derivatives.

Solubility
Miscible with water.

Notes
Hygroscopic. Incompatible with strong oxidizing agents, sulfuric acid, acids, metals, iron(II) sulfate and hydrogen peroxide.
RUO – Research Use Only

General References:

  1. Dhau, J. S.; Singh, A. A study on the BF3-directed lithiation of 2-picoline and 2,3-lutidine. J. Organomet. Chem. 2014, 749, 109-114.
  2. Li, B.; Wei, H.; Li, H.; Pereshivko, O. P.; Peshkov, V. A. Direct addition of 2-methylazines to aryl glyoxals for the synthesis of alpha-hydroxy ketones. Tetrahedron Lett. 2015, 56 (37), 5231-5234.