L-Proline tert-butyl ester hydrochloride
98%
- Product Code: 105345
CAS:
5497-76-7
Molecular Weight: | 207.7 g./mol | Molecular Formula: | C₉H₁₇NO₂HCl |
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EC Number: | 226-835-2 | MDL Number: | MFCD00153459 |
Melting Point: | 110-112°C | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
L-Proline tert-butyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-proline, enabling the selective formation of peptide bonds without unwanted side reactions. This compound is valuable in the production of complex peptides and proteins, where it helps maintain the integrity of the proline residue during synthesis. Additionally, it is utilized in the development of pharmaceuticals, especially in the creation of drugs targeting neurological and cardiovascular disorders. Its stability and ease of deprotection make it a preferred choice in solid-phase peptide synthesis and other advanced chemical processes.
Product Specification:
Test | Specification |
---|---|
Appearance | White To Almost White Powder To Crystal |
Purity (%) | 97.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Melting Point (Degree Celsius) | 109-114 |
Specific Rotation [α]20/D(C=1, H2O) | -30 Degree -33 Degree |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | £8.82 |
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5.000 | 10-20 days | £27.59 |
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25.000 | 10-20 days | £118.06 |
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L-Proline tert-butyl ester hydrochloride
L-Proline tert-butyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-proline, enabling the selective formation of peptide bonds without unwanted side reactions. This compound is valuable in the production of complex peptides and proteins, where it helps maintain the integrity of the proline residue during synthesis. Additionally, it is utilized in the development of pharmaceuticals, especially in the creation of drugs targeting neurological and cardiovascular disorders. Its stability and ease of deprotection make it a preferred choice in solid-phase peptide synthesis and other advanced chemical processes.
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