N-(tert-Butoxycarbonyl)-D-3-chlorophenylalanine
98%
- Product Code: 105533
Alias:
N-tert-butoxycarbonyl-D-3-chlorophenylalanine
CAS:
80102-25-6
| Molecular Weight: | 299.75 g./mol | Molecular Formula: | C₁₄H₁₈ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672516 | |
| Melting Point: | 110°C | Boiling Point: | |
| Density: | 1.245 | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used in the synthesis of peptides and pharmaceutical compounds, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled reactions during peptide synthesis, ensuring the desired sequence and structure are achieved. The presence of the chlorophenyl group enhances its utility in creating molecules with specific binding properties, often used in the study of enzyme inhibitors or receptor modulators. It is also employed in research focused on developing treatments for neurological disorders, as its structure can mimic natural amino acids involved in brain function. Additionally, it serves as a key intermediate in the production of chiral compounds, which are essential in asymmetric synthesis for creating enantiomerically pure drugs.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,810.00 |
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| 5.000 | 10-20 days | ฿6,880.00 |
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N-(tert-Butoxycarbonyl)-D-3-chlorophenylalanine
This chemical is widely used in the synthesis of peptides and pharmaceutical compounds, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled reactions during peptide synthesis, ensuring the desired sequence and structure are achieved. The presence of the chlorophenyl group enhances its utility in creating molecules with specific binding properties, often used in the study of enzyme inhibitors or receptor modulators. It is also employed in research focused on developing treatments for neurological disorders, as its structure can mimic natural amino acids involved in brain function. Additionally, it serves as a key intermediate in the production of chiral compounds, which are essential in asymmetric synthesis for creating enantiomerically pure drugs.
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