4-Bromothiophenol

97%

  • Product Code: 119401
  Alias:    4-Bromothiophenol
  CAS:    106-53-6
Molecular Weight: 189.07 g./mol Molecular Formula: BrC₆H₄SH
EC Number: 203-407-3 MDL Number: MFCD00004845
Melting Point: 73-76 °C(lit.) Boiling Point: 239 °C(lit.)
Density: Storage Condition: 2~8°C
Product Description: 4-Bromothiophenol finds its primary application in organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine and thiol functional groups make it a valuable building block for constructing complex molecules, particularly in the development of sulfur-containing compounds. Additionally, it is used in the synthesis of ligands for catalysis and in the preparation of polymers with specific electronic or optical properties. Its reactivity also allows it to act as a precursor in the creation of dyes and pigments. In research, 4-Bromothiophenol is employed in the study of thiol-based reactions and as a model compound for investigating sulfur chemistry.
Product Specification:
Test Specification
Melting Point 73-76
Purity (T) 96.5-103.5
Purity (GC) 97-100
Appearance White To Yellow Powder Or Crystals
Infrared Spectrum Conforms To Structure
Solubility In Methanol Very Faint Turbidity
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿320.00
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5.000 10-20 days ฿680.00
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25.000 10-20 days ฿1,680.00
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100.000 10-20 days ฿5,980.00
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500.000 10-20 days ฿18,690.00
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4-Bromothiophenol
4-Bromothiophenol finds its primary application in organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromine and thiol functional groups make it a valuable building block for constructing complex molecules, particularly in the development of sulfur-containing compounds. Additionally, it is used in the synthesis of ligands for catalysis and in the preparation of polymers with specific electronic or optical properties. Its reactivity also allows it to act as a precursor in the creation of dyes and pigments. In research, 4-Bromothiophenol is employed in the study of thiol-based reactions and as a model compound for investigating sulfur chemistry.
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