S-Benzylisothiourea hydrochloride

98.5%

  • Product Code: 121675
  Alias:    S-benzylisothiourea hydrochloride ;benzylisothiourea hydrochloride,benzylisothiourea hydrochloride,hydrochloride-S-benzylisothiourea
  CAS:    538-28-3
Molecular Weight: 202.7 g./mol Molecular Formula: C₈H₁₀N₂SHCl
EC Number: 208-688-6 MDL Number: MFCD00012583
Melting Point: 172-177 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: S-Benzylisothiourea hydrochloride is widely used in organic synthesis as a reagent for the preparation of thiols and sulfides. It serves as a key intermediate in the production of various pharmaceuticals, particularly in the synthesis of compounds with potential antimicrobial and antiviral properties. The chemical is also employed in the development of peptide mimetics and enzyme inhibitors, where its thiourea moiety plays a critical role in binding interactions. Additionally, it finds application in the modification of biomolecules and polymers, enhancing their functional properties for use in drug delivery systems and material science. Its ability to act as a protecting group for thiols further extends its utility in complex synthetic pathways.
Product Specification:
Test Specification
Assay 98.5-100
Melting Point 175 Degree Celsius-178 Degree Celsius
Appearance White To Light Yellow Powder
Solubility In Water Pass
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿330.00
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5.000 10-20 days ฿630.00
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25.000 10-20 days ฿1,950.00
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-
100.000 10-20 days ฿5,610.00
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500.000 10-20 days ฿22,680.00
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S-Benzylisothiourea hydrochloride
S-Benzylisothiourea hydrochloride is widely used in organic synthesis as a reagent for the preparation of thiols and sulfides. It serves as a key intermediate in the production of various pharmaceuticals, particularly in the synthesis of compounds with potential antimicrobial and antiviral properties. The chemical is also employed in the development of peptide mimetics and enzyme inhibitors, where its thiourea moiety plays a critical role in binding interactions. Additionally, it finds application in the modification of biomolecules and polymers, enhancing their functional properties for use in drug delivery systems and material science. Its ability to act as a protecting group for thiols further extends its utility in complex synthetic pathways.
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