1-Phenyl-2-thiocyanatoethanone
95%
- Product Code: 81710
CAS:
5399-30-4
Molecular Weight: | 177.22 g./mol | Molecular Formula: | C₉H₇NOS |
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EC Number: | MDL Number: | MFCD00019769 | |
Melting Point: | 74.1-74.6 °C (lit.) | Boiling Point: | 331.5 °C at 760 mmHg (lit.) |
Density: | Storage Condition: | 2-8°C, dry |
Product Description:
1-Phenyl-2-thiocyanatoethanone is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. The thiocyanate group in the molecule makes it a valuable precursor for the synthesis of thiazoles and other sulfur-containing heterocycles, which are known for their biological activities. Additionally, it is used in the synthesis of organic dyes and pigments, contributing to the production of colorants for textiles and plastics. Its reactivity with nucleophiles also makes it a useful reagent in the construction of complex organic molecules, particularly in the field of medicinal chemistry where it aids in the creation of potential drug candidates.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿8,883.00 |
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1-Phenyl-2-thiocyanatoethanone
1-Phenyl-2-thiocyanatoethanone is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. The thiocyanate group in the molecule makes it a valuable precursor for the synthesis of thiazoles and other sulfur-containing heterocycles, which are known for their biological activities. Additionally, it is used in the synthesis of organic dyes and pigments, contributing to the production of colorants for textiles and plastics. Its reactivity with nucleophiles also makes it a useful reagent in the construction of complex organic molecules, particularly in the field of medicinal chemistry where it aids in the creation of potential drug candidates.
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