2-Methoxybenzenesulfonyl chloride, 95%
2-Methoxybenzenesulfonyl chloride, 95%
2-Methoxybenzenesulfonyl chloride, 95%
Thermo Scientific Chemicals

2-Methoxybenzenesulfonyl chloride, 95%

CAS: 10130-87-7 | C7H7ClO3S | 206.64 g/mol
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Catalog NumberQuantity
H34455.03
also known as H34455-03
1 g
Catalog number H34455.03
also known as H34455-03
Price (EUR)
134,00
Each
Quantity:
1 g
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Price (EUR)
134,00
Each
Chemical Identifiers
CAS10130-87-7
IUPAC Name2-methoxybenzene-1-sulfonyl chloride
Molecular FormulaC7H7ClO3S
InChI KeyGYOBZOBUOMDRRN-UHFFFAOYSA-N
SMILESCOC1=CC=CC=C1S(Cl)(=O)=O
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Appearance (Color)White to pale cream
Assay (GC)≥94.0%
Melting Point (clear melt)50.5-59.5?C
For synthesis and pharmacological evaluation of sulfonamide derivatives of thiazolidin-4-ones 5-Bromo-2-methoxybenzenesulfonyl chloride is used.

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
For synthesis and pharmacological evaluation of sulfonamide derivatives of thiazolidin-4-ones 5-Bromo-2-methoxybenzenesulfonyl chloride is used.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture, bases.
RUO – Research Use Only

General References:

  1. Nadeem Siddiqui,; M. Faiz Arshad,; Suroor A. Khana,; Waquar Ahsana. Sulfonamide derivatives of thiazolidin-4-ones with anticonvulsant activity against two seizure models: synthesis and pharmacological evaluation. Journal of Enzyme Inhibition and Medicinal Chemistry. 2010, 25(4),485-491.
  2. Valeria De Matteis,; Floris L. van Delft,; Harald Jakobi,; Stephen Lindell,; Jörg Tiebes,; Floris P. J. T. Rutjes. RCM-Mediated Synthesis of Trifluoromethyl-Containing Nitrogen Heterocycles. J. Org. Chem.,. 2006, 71 (20), 7527-7532.