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2-Aminothiophenol, 98%, Thermo Scientific Chemicals
Catalog number: A18952.36
500 g, Each
Thermo Scientific Chemicals
2-Aminothiophenol, 98%, Thermo Scientific Chemicals
Catalog number: A18952.36
500 g, Each
Quantity
Catalog number: A18952.36
also known as A18952-36
Price (USD)
Price: 196.00
Online price: 166.65
Your price:
Quantity
-
Chemical Identifiers
CAS
137-07-5
IUPAC Name
2-aminobenzene-1-thiol
Molecular Formula
C6H7NS
InChI Key
VRVRGVPWCUEOGV-UHFFFAOYSA-N
SMILES
NC1=CC=CC=C1S
Specifications
Specification SheetIdentification (FTIR)
Conforms
Form
Crystals or powder or crystalline powder or fused solid or clear liquid as melt
Refractive Index
1.6405-1.6445 @ 20?C
Appearance (Color)
Yellow to brown
Assay (GC)
≥97.5%
Description
2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of copper (II) with salicylidene-2-aminothiophenol (L) and glycine, alanine, valine and histidene amino acids.
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-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of copper (II) with salicylidene-2-aminothiophenol (L) and glycine, alanine, valine and histidene amino acids.
Solubility
Insoluble in water.
Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, air.
2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of copper (II) with salicylidene-2-aminothiophenol (L) and glycine, alanine, valine and histidene amino acids.
Solubility
Insoluble in water.
Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, air.
RUO – Research Use Only
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