L-Phenylalanine tert-butyl ester hydrochloride
98%
- Product Code: 105359
Alias:
L-phenylalanine tert-butyl hydrochloride
CAS:
15100-75-1
| Molecular Weight: | 257.76 g./mol | Molecular Formula: | C₁₃H₁₉NO₂HCl |
|---|---|---|---|
| EC Number: | 239-151-4 | MDL Number: | MFCD00038894 |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
L-Phenylalanine tert-butyl ester hydrochloride is primarily used in peptide synthesis, where it serves as a protected form of L-phenylalanine. Its tert-butyl ester group provides stability during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides by ensuring the amino acid remains intact until the final deprotection step. Additionally, it is utilized in the preparation of chiral intermediates for pharmaceutical applications, contributing to the production of enantiomerically pure drugs. Its role in organic synthesis extends to the development of bioactive molecules and complex organic compounds, making it a versatile reagent in both academic and industrial research settings.
Product Specification:
| Test | Specification |
|---|---|
| Optical Activity | 45-49 |
| Purity (%) | 97.5-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿290.00 |
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| 5.000 | 10-20 days | ฿500.00 |
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| 25.000 | 10-20 days | ฿1,980.00 |
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| 100.000 | 10-20 days | ฿6,380.00 |
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L-Phenylalanine tert-butyl ester hydrochloride
L-Phenylalanine tert-butyl ester hydrochloride is primarily used in peptide synthesis, where it serves as a protected form of L-phenylalanine. Its tert-butyl ester group provides stability during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides by ensuring the amino acid remains intact until the final deprotection step. Additionally, it is utilized in the preparation of chiral intermediates for pharmaceutical applications, contributing to the production of enantiomerically pure drugs. Its role in organic synthesis extends to the development of bioactive molecules and complex organic compounds, making it a versatile reagent in both academic and industrial research settings.
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