Fmoc-N-(2,4,6-trimethoxybenzyl)-glycine
97%
- Product Code: 50308
CAS:
166881-43-2
| Molecular Weight: | 477.51 g./mol | Molecular Formula: | C₂₇H₂₇NO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09952622 | |
| Melting Point: | Boiling Point: | 676.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected glycine derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, while the 2,4,6-trimethoxybenzyl (Tmob) group protects the carboxylic acid functionality. This dual protection allows for selective deprotection and coupling steps, enabling the controlled assembly of peptide chains. Its application is crucial in the synthesis of complex peptides and proteins, which are widely used in pharmaceutical research, drug development, and biochemical studies. Additionally, it is employed in the preparation of peptide libraries for high-throughput screening in drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿333.00 |
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| 0.250 | 10-20 days | ฿486.00 |
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| 1.000 | 10-20 days | ฿1,215.00 |
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Fmoc-N-(2,4,6-trimethoxybenzyl)-glycine
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected glycine derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, while the 2,4,6-trimethoxybenzyl (Tmob) group protects the carboxylic acid functionality. This dual protection allows for selective deprotection and coupling steps, enabling the controlled assembly of peptide chains. Its application is crucial in the synthesis of complex peptides and proteins, which are widely used in pharmaceutical research, drug development, and biochemical studies. Additionally, it is employed in the preparation of peptide libraries for high-throughput screening in drug discovery processes.
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