1-Phenyl-3-thiosemicarbazide
≥98%
Reagent
Code: #114936
CAS Number
645-48-7
blur_circular Chemical Specifications
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Molecular Information
Weight
167.23 g/mol
Formula
C₇H₉N₃S
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Registry Numbers
MDL Number
MFCD00042739
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Storage & Handling
Storage
room temperature
description Product Description
Primarily used in organic synthesis, this compound serves as a key intermediate in the preparation of various heterocyclic compounds. It is particularly valuable in the synthesis of thiadiazoles, which have applications in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of corrosion inhibitors for metals, offering protection in industrial environments. Its role in coordination chemistry is also notable, where it acts as a ligand to form complexes with transition metals, useful in catalysis and material science. Furthermore, it finds use in analytical chemistry as a reagent for the detection and quantification of certain metal ions.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to light yellow to light orange powder to crystal |
Purity (%) | 97.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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1-Phenyl-3-thiosemicarbazide
Primarily used in organic synthesis, this compound serves as a key intermediate in the preparation of various heterocyclic compounds. It is particularly valuable in the synthesis of thiadiazoles, which have applications in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of corrosion inhibitors for metals, offering protection in industrial environments. Its role in coordination chemistry is also notable, where it acts as a ligand to form complexes with transition metals, useful in catalysis and material science. Furthermore, it finds use in analytical chemistry as a reagent for the detection and quantification of certain metal ions.
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