tert-butyl N-[(2R)-1-amino-3-methyl-1-oxobutan-2-yl]carbamate
95%
- Product Code: 104718
CAS:
70717-76-9
Molecular Weight: | 216.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₃ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 361.7ºC at 760 mmHg | |
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the synthesis of peptides and proteins, serving as a protecting group for amino acids during organic synthesis. It plays a crucial role in peptide coupling reactions, ensuring the selective protection of specific functional groups to prevent unwanted side reactions. Its application is particularly valuable in the production of complex peptides, including those used in pharmaceutical research and drug development. Additionally, it is utilized in the preparation of intermediates for bioactive compounds, contributing to the development of therapeutic agents targeting various diseases. Its stability and compatibility with various reaction conditions make it a reliable choice in solid-phase peptide synthesis and other organic transformations.
Product Specification:
Test | Specification |
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Appearance | Colourless To White Solid |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿2,300.00 |
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5.000 | 10-20 days | ฿6,500.00 |
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25.000 | 10-20 days | ฿20,100.00 |
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tert-butyl N-[(2R)-1-amino-3-methyl-1-oxobutan-2-yl]carbamate
This chemical is primarily used in the synthesis of peptides and proteins, serving as a protecting group for amino acids during organic synthesis. It plays a crucial role in peptide coupling reactions, ensuring the selective protection of specific functional groups to prevent unwanted side reactions. Its application is particularly valuable in the production of complex peptides, including those used in pharmaceutical research and drug development. Additionally, it is utilized in the preparation of intermediates for bioactive compounds, contributing to the development of therapeutic agents targeting various diseases. Its stability and compatibility with various reaction conditions make it a reliable choice in solid-phase peptide synthesis and other organic transformations.
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