tert-Butyl isothiocyanate

99%

  • Product Code: 122363
  Alias:    tert-butyl isothiocyanate; tert-butyl isothiocyanate, tert-butyl isothiocyanate
  CAS:    590-42-1
Molecular Weight: 115.2 g./mol Molecular Formula: C₅H₉NS
EC Number: 209-682-6 MDL Number: MFCD00004816
Melting Point: 8-11 °C Boiling Point: 141-145 °C
Density: 0.908 Storage Condition: room temperature, flammable area
Product Description: Used primarily in organic synthesis, it serves as a key intermediate in the production of various heterocyclic compounds. It is also employed in the development of agrochemicals, particularly in the creation of pesticides and herbicides. In the pharmaceutical industry, it is utilized in the synthesis of potential drug candidates, especially those targeting cancer and other diseases. Additionally, it finds application in research laboratories for studying biochemical pathways and enzyme inhibition mechanisms. Its reactivity with amines and other nucleophiles makes it valuable in the preparation of thiourea derivatives, which have diverse industrial and medicinal uses.
Product Specification:
Test Specification
Purity (GC) 99
Refractive Index N20/D 1.48-1.482
Specific Gravity (20/20 Degree Celsius) 0.907-0.909
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days £22.84
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25.000 10-20 days £78.93
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100.000 10-20 days £225.94
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tert-Butyl isothiocyanate
Used primarily in organic synthesis, it serves as a key intermediate in the production of various heterocyclic compounds. It is also employed in the development of agrochemicals, particularly in the creation of pesticides and herbicides. In the pharmaceutical industry, it is utilized in the synthesis of potential drug candidates, especially those targeting cancer and other diseases. Additionally, it finds application in research laboratories for studying biochemical pathways and enzyme inhibition mechanisms. Its reactivity with amines and other nucleophiles makes it valuable in the preparation of thiourea derivatives, which have diverse industrial and medicinal uses.
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