4-[(tert-Butoxycarbonyl)amino]cyclohexanol (Mixture of Diastereomers)

97%

  • Product Code: 85405
  Alias:    4-(Boc-amino)cyclohexanol; tert-butyl (4-hydroxycyclohexyl)carbamate
  CAS:    224309-64-2
Molecular Weight: 215.29 g./mol Molecular Formula: C₁₁H₂₁NO₃
EC Number: MDL Number: MFCD06658349
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, sealed
Product Description: This compound is widely used in organic synthesis as a protected intermediate in the preparation of pharmaceuticals and bioactive molecules. Its tert-butoxycarbonyl (Boc) group serves as a protective moiety for the amine functionality, allowing selective reactions to occur on other parts of the molecule without interference. It is particularly valuable in peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, the cyclohexanol structure provides a rigid framework, making it useful in the design of compounds with specific stereochemical properties. Its mixture of diastereomers can be separated and utilized to explore stereoselective reactions, contributing to the development of chiral drugs and fine chemicals.
Product Specification:
Test Specification
Purity 96.5-100
Melting point 170-174
Appearance White to light yellow
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿360.00
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5.000 10-20 days ฿900.00
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-
25.000 10-20 days ฿2,590.00
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-
100.000 10-20 days ฿9,630.00
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4-[(tert-Butoxycarbonyl)amino]cyclohexanol (Mixture of Diastereomers)
This compound is widely used in organic synthesis as a protected intermediate in the preparation of pharmaceuticals and bioactive molecules. Its tert-butoxycarbonyl (Boc) group serves as a protective moiety for the amine functionality, allowing selective reactions to occur on other parts of the molecule without interference. It is particularly valuable in peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, the cyclohexanol structure provides a rigid framework, making it useful in the design of compounds with specific stereochemical properties. Its mixture of diastereomers can be separated and utilized to explore stereoselective reactions, contributing to the development of chiral drugs and fine chemicals.
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