(9H-Fluoren-9-yl)methyl ((2S,3S)-1-chloro-3-methyl-1-oxopentan-2-yl)carbamate
95%
- Product Code: 191236
CAS:
103321-51-3
| Molecular Weight: | 371.85 g./mol | Molecular Formula: | C₂₁H₂₂NO₃Cl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00235816 | |
| Melting Point: | 101-103 °C | Boiling Point: | 518.8±33.0 °C(Predicted) |
| Density: | 1.213±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as a chiral derivatizing agent in organic synthesis, particularly in the preparation of peptide mimetics and enzyme inhibitors. Its structure allows for selective protection of amino groups in asymmetric synthesis, making it valuable in pharmaceutical research for developing optically active compounds. Commonly employed in solid-phase peptide synthesis due to the stability and ease of removal of the fluorenylmethyl carbamate (Fmoc) group under mild basic conditions. The chloroacyl moiety enables further functionalization, facilitating the construction of complex molecules with defined stereochemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿2,320.00 |
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| 5.000 G | 10-20 days | ฿7,920.00 |
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(9H-Fluoren-9-yl)methyl ((2S,3S)-1-chloro-3-methyl-1-oxopentan-2-yl)carbamate
Used as a chiral derivatizing agent in organic synthesis, particularly in the preparation of peptide mimetics and enzyme inhibitors. Its structure allows for selective protection of amino groups in asymmetric synthesis, making it valuable in pharmaceutical research for developing optically active compounds. Commonly employed in solid-phase peptide synthesis due to the stability and ease of removal of the fluorenylmethyl carbamate (Fmoc) group under mild basic conditions. The chloroacyl moiety enables further functionalization, facilitating the construction of complex molecules with defined stereochemistry.
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