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1-(p-Toluenesulfonyl)indole, 95%, Thermo Scientific Chemicals
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Catalog number B22320.06
also known as B22320-06
Price (USD)/ Each
224.00
-
Quantity:
5 g
Price (USD)/ Each
224.00
1-(p-Toluenesulfonyl)indole, 95%, Thermo Scientific Chemicals
Catalog numberB22320.06
Price (USD)/ Each
224.00
-
Chemical Identifiers
CAS31271-90-6
IUPAC Name1-(4-methylbenzenesulfonyl)-1H-indole
Molecular FormulaC15H13NO2S
InChI KeyJNRRPYFLDADLJW-UHFFFAOYSA-N
SMILESCC1=CC=C(C=C1)S(=O)(=O)N1C=CC2=CC=CC=C12
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream
Melting Point (clear melt)79.0-91.0?C
Assay (GC)≥94.0%
FormPowder
1-(p-Toluenesulfonyl)indole, is synthesized and used as a stable equivalent of 4-mercaptoindoles, also used in medicinal field for making drug and tablets.
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
1-(p-Toluenesulfonyl)indole, is synthesized and used as a stable equivalent of 4-mercaptoindoles, also used in medicinal field for making drug and tablets.
Solubility
Insoluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
1-(p-Toluenesulfonyl)indole, is synthesized and used as a stable equivalent of 4-mercaptoindoles, also used in medicinal field for making drug and tablets.
Solubility
Insoluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
General References:
- Terry V. Hughes.; Michael P. Cava. Electrophilic Cyanations Using 1-Cyanobenzotriazole: sp2 and sp Carbanions. J. Org. Chem. 1999, 64, (1), 313-315.
- Gerald S. Ponticello.; John J. Baldwin. Useful synthesis of 4-substituted indoles. J. Org. Chem.1979, 44, (22), 4003-4005.