Boc-allyl-Gly-OH (dicyclohexylammonium) salt
98%
- Product Code: 104855
Alias:
2-Allyl-N-Boc-L-aminoacetic acid dicyclohexylammonium salt
CAS:
143979-15-1
| Molecular Weight: | 396.56 g./mol | Molecular Formula: | C₁₀H₁₇NO₄C₁₂H₂₃N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321013 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
Boc-allyl-Gly-OH (dicyclohexylammonium) salt is primarily used in peptide synthesis as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, preventing unwanted reactions during the synthesis process. The allyl group offers additional versatility, as it can be selectively removed under mild conditions, allowing for further functionalization or deprotection steps. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where controlled and sequential coupling of amino acids is required. Its stability and ease of handling make it a preferred choice for researchers and industrial applications in the production of peptides, which are widely used in pharmaceuticals, biotechnology, and biochemical research.
Product Specification:
| Test | Specification |
|---|---|
| Purity (NT) | 97.5-102.5 |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿660.00 |
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| 1.000 | 10-20 days | ฿1,790.00 |
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| 5.000 | 10-20 days | ฿5,540.00 |
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| 25.000 | 10-20 days | ฿23,680.00 |
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Boc-allyl-Gly-OH (dicyclohexylammonium) salt
Boc-allyl-Gly-OH (dicyclohexylammonium) salt is primarily used in peptide synthesis as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, preventing unwanted reactions during the synthesis process. The allyl group offers additional versatility, as it can be selectively removed under mild conditions, allowing for further functionalization or deprotection steps. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, where controlled and sequential coupling of amino acids is required. Its stability and ease of handling make it a preferred choice for researchers and industrial applications in the production of peptides, which are widely used in pharmaceuticals, biotechnology, and biochemical research.
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