(2S,3S)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylpentanoic acid
95%
- Product Code: 52227
CAS:
52498-32-5
| Molecular Weight: | 245.32 g./mol | Molecular Formula: | C₁₂H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066105 | |
| Melting Point: | Boiling Point: | 338.2°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in the field of organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a key intermediate in the development of complex molecules, often employed in the synthesis of biologically active compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, where selective protection and deprotection of functional groups are essential. Additionally, it is utilized in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting specific enzymes or receptors. The compound’s chiral centers also make it useful in asymmetric synthesis, contributing to the production of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,538.00 |
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| 5.000 | 10-20 days | ฿7,866.00 |
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| 10.000 | 10-20 days | ฿13,140.00 |
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(2S,3S)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylpentanoic acid
This chemical is primarily used in the field of organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a key intermediate in the development of complex molecules, often employed in the synthesis of biologically active compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, where selective protection and deprotection of functional groups are essential. Additionally, it is utilized in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting specific enzymes or receptors. The compound’s chiral centers also make it useful in asymmetric synthesis, contributing to the production of enantiomerically pure substances.
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