O-Tritylhydroxylamine
97%
- Product Code: 56383
CAS:
31938-11-1
Molecular Weight: | 275.34 g./mol | Molecular Formula: | C₁₉H₁₇NO |
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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 |
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Purity | 97-100 |
MELTING POINT | 75-88 |
APPEARANCE | SOLID |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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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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