O-Tritylhydroxylamine

97%

  • Product Code: 56383
  CAS:    31938-11-1
Molecular Weight: 275.34 g./mol Molecular Formula: C₁₉H₁₇NO
EC Number: MDL Number:
Melting Point: 79-81°C Boiling Point: 443.2°C
Density: Storage Condition: 2-8°C
Product Description: O-Tritylhydroxylamine is widely used in organic synthesis as a protecting group for hydroxylamine. It is particularly valuable in the preparation of complex molecules, where selective protection and deprotection of functional groups are required. This compound is often employed in the synthesis of pharmaceuticals and agrochemicals, where it helps to stabilize sensitive intermediates during multi-step reactions. In peptide chemistry, O-Tritylhydroxylamine is utilized to protect hydroxylamine derivatives, enabling the controlled formation of peptide bonds without unwanted side reactions. It also finds application in the development of heterocyclic compounds, where it acts as a key intermediate in the construction of nitrogen-containing rings. Additionally, it is used in the synthesis of oxime ethers, which are important in the production of various bioactive molecules. Its ability to be easily removed under mild conditions makes it a versatile tool in synthetic chemistry.
Product Specification:
Test Specification
Purity 97-100
MELTING POINT 75-88
APPEARANCE SOLID
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $7.50
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1.000 10-20 days $9.90
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5.000 10-20 days $30.30
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O-Tritylhydroxylamine
O-Tritylhydroxylamine is widely used in organic synthesis as a protecting group for hydroxylamine. It is particularly valuable in the preparation of complex molecules, where selective protection and deprotection of functional groups are required. This compound is often employed in the synthesis of pharmaceuticals and agrochemicals, where it helps to stabilize sensitive intermediates during multi-step reactions. In peptide chemistry, O-Tritylhydroxylamine is utilized to protect hydroxylamine derivatives, enabling the controlled formation of peptide bonds without unwanted side reactions. It also finds application in the development of heterocyclic compounds, where it acts as a key intermediate in the construction of nitrogen-containing rings. Additionally, it is used in the synthesis of oxime ethers, which are important in the production of various bioactive molecules. Its ability to be easily removed under mild conditions makes it a versatile tool in synthetic chemistry.
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