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Thermo Scientific Chemicals
Thiobenzamide, 98%
CAS: 2227-79-4 | C7H7NS | 137.20 g/mol
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Catalog number A12973.22
also known as A12973-22
Price (EUR)
117,00
Each
Quantity:
100 g
Price (EUR)
117,00
Each
Chemical Identifiers
CAS2227-79-4
IUPAC Namebenzenecarbothioamide
Molecular FormulaC7H7NS
InChI KeyQIOZLISABUUKJY-UHFFFAOYSA-N
SMILESNC(=S)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Pale yellow to yellow to green
FormPowder
Assay (GC)≥97.5%
Melting Point (clear melt)113.0-121.0?C
Thiobenzamide is useful for the preparation of amide and amidine adducts. It is also used to prepare 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides. Further, it acts as a raw material in organic synthesis.
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
Thiobenzamide is useful for the preparation of amide and amidine adducts. It is also used to prepare 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides. Further, it acts as a raw material in organic synthesis.
Solubility
Slightly soluble in water.
Notes
Incompatible with strong oxidizing agents and strong bases.
Thiobenzamide is useful for the preparation of amide and amidine adducts. It is also used to prepare 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides. Further, it acts as a raw material in organic synthesis.
Solubility
Slightly soluble in water.
Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Long, T. R.; Wongrakpanich, A.; Do, A. V.; Salem, A. K.; Bowden, N. B. Long-term release of a thiobenzamide from a backbone functionalized poly(lactic acid). Polym. Chem. 2015, 6 (40), 7188-7195.
- Nahakpam, L.; Chipem, F. A. S.; Chingakham, B. S.; Laitonjam, W. S. Decomposition of benzoylthioureas into benzamides and thiobenzamides under solvent-free conditions using iodine-alumina as the catalyst and its mechanistic study by density functional theory. New J. Chem. 2015, 39 (3), 2240-2247.