O-Benzyl-L-serine
99%
- Product Code: 59235
Alias:
O-Benzyl-L-serine
CAS:
4726-96-9
Molecular Weight: | 195.22 g./mol | Molecular Formula: | C₁₀H₁₃NO₃ |
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EC Number: | 225-220-6 | MDL Number: | MFCD00065937 |
Melting Point: | ~227 °C (dec.) | Boiling Point: | 359℃ |
Density: | 1.217 | Storage Condition: | room temperature |
Product Description:
O-Benzyl-L-serine is widely used in the synthesis of peptides and proteins, serving as a protected form of serine. Its benzyl group acts as a protective moiety, preventing unwanted reactions during peptide bond formation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required to build complex peptide structures. It is also employed in the development of pharmaceutical compounds, especially in the creation of serine-based drugs or enzyme inhibitors. Additionally, O-Benzyl-L-serine is utilized in biochemical research to study enzyme mechanisms and protein interactions, owing to its ability to mimic natural serine in controlled environments. Its stability and reactivity make it a key intermediate in organic and medicinal chemistry applications.
Product Specification:
Test | Specification |
---|---|
PURITYNONAQUEOUS TIERATION | 99 100% |
HCL | 6.5-8 |
APPEARANCE | White to off-white powder or solid or chunks |
INFRARED SPECTROMETRY | Conforms to Structure |
SOLUBILITY IN HOT WATER | almost transparency |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿450.00 |
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5.000 | 10-20 days | ฿1,460.00 |
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25.000 | 10-20 days | ฿6,610.00 |
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O-Benzyl-L-serine
O-Benzyl-L-serine is widely used in the synthesis of peptides and proteins, serving as a protected form of serine. Its benzyl group acts as a protective moiety, preventing unwanted reactions during peptide bond formation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required to build complex peptide structures. It is also employed in the development of pharmaceutical compounds, especially in the creation of serine-based drugs or enzyme inhibitors. Additionally, O-Benzyl-L-serine is utilized in biochemical research to study enzyme mechanisms and protein interactions, owing to its ability to mimic natural serine in controlled environments. Its stability and reactivity make it a key intermediate in organic and medicinal chemistry applications.
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