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Thermo Scientific Chemicals
Thiophene-2-sulfonyl chloride, 97%
CAS: 16629-19-9 | C4H3ClO2S2 | 182.64 g/mol
化学物質識別子
CAS16629-19-9
IUPAC Namethiophene-2-sulfonyl chloride
Molecular FormulaC4H3ClO2S2
InChI KeyVNNLHYZDXIBHKZ-UHFFFAOYSA-N
SMILESClS(=O)(=O)C1=CC=CS1
さらに表示
仕様
スペックシート
スペックシートFormCrystals or powder or crystalline powder or chunks or fused solid
Melting Point (clear melt)26.0-35.0?C
Appearance (Color)White to orange or blue to pale gray to gray to black
Assay (GC)≥96.0%
2-Thiophenesulfonyl chloride has been used in the preparation of 2-((trans-2-phenyl cyclopropyl)sulfonyl)thiophene
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-Thiophenesulfonyl chloride has been used in the preparation of 2-((trans-2-phenyl cyclopropyl)sulfonyl)thiophene
Solubility
Reacts with water.
Notes
Moisture sensitive. Store under inert gas. Store away from moisture, oxidizing agents, bases.
2-Thiophenesulfonyl chloride has been used in the preparation of 2-((trans-2-phenyl cyclopropyl)sulfonyl)thiophene
Solubility
Reacts with water.
Notes
Moisture sensitive. Store under inert gas. Store away from moisture, oxidizing agents, bases.
RUO – Research Use Only
General References:
- Aránzazu Sánchez; Araceli Núñez; Julio Alvarez-Builla; Carolina Burgos. Pyridinium N-2'-pyridylaminide: synthesis of 3-aryl-2-aminopyridines through an intramolecular radical process. Tetrahedron. 2004, 60 (51), 11843-11850.
- Richard J. Cremlyn; Kenneth H. Goulding; Frederick J. Swinbourne & Kin-Man Yung. The Reactions Of Some Thiophene Sulfonyl Derivatives. Phosphorus and Sulfur and the Related Elements. 1981, 10 (1), 111-119.