L-Proline benzyl ester hydrochloride
98%
- Product Code: 105347
Alias:
L-Proline Benzyl Ester Hydrochloride
CAS:
16652-71-4
Molecular Weight: | 241.71 g./mol | Molecular Formula: | C₁₂H₁₅NO₂HCl |
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EC Number: | 240-700-5 | MDL Number: | MFCD00039002 |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, sealed |
Product Description:
L-Proline benzyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-proline, where the benzyl ester group helps in preventing unwanted reactions during peptide bond formation. This compound is essential in the synthesis of complex peptides and proteins, ensuring the integrity of the proline residue. Additionally, it is utilized in the preparation of chiral catalysts and intermediates for pharmaceuticals, contributing to the production of enantiomerically pure compounds. Its role in asymmetric synthesis is also notable, aiding in the development of drugs and bioactive molecules with high stereochemical precision.
Product Specification:
Test | Specification |
---|---|
D-Enantiomer | 0-0.5 |
Melting Point | 142 Degree Celsius-148 Degree Celsius |
Purity (HPLC) | 98-100 |
Specific Rotation [A]20/D(C=1 In Meoh) | 43-45 |
Appearance | White Crystal Powder |
TLC Analysis | One Spot |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿460.00 |
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25.000 | 10-20 days | ฿1,120.00 |
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100.000 | 10-20 days | ฿3,600.00 |
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L-Proline benzyl ester hydrochloride
L-Proline benzyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-proline, where the benzyl ester group helps in preventing unwanted reactions during peptide bond formation. This compound is essential in the synthesis of complex peptides and proteins, ensuring the integrity of the proline residue. Additionally, it is utilized in the preparation of chiral catalysts and intermediates for pharmaceuticals, contributing to the production of enantiomerically pure compounds. Its role in asymmetric synthesis is also notable, aiding in the development of drugs and bioactive molecules with high stereochemical precision.
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