(S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate
97%
- Product Code: 236627
CAS:
1374635-44-5
| Molecular Weight: | 350.45 g./mol | Molecular Formula: | C₁₉H₃₀N₂O₄ |
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| EC Number: | MDL Number: | MFCD34165719 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed |
Product Description:
Used as a chiral protecting group reagent in organic synthesis, particularly in the preparation of enantiomerically pure compounds. Its main application lies in peptide synthesis and the construction of complex molecules where stereochemical control is critical. The tert-butyl carbamate (Boc) groups provide orthogonal protection for amines, allowing selective deprotection under mild acidic conditions without affecting other sensitive functional groups. The benzyl group can be removed selectively via hydrogenolysis, enabling stepwise assembly of multifunctional molecules. Commonly employed in pharmaceutical research for synthesizing chiral intermediates, especially in the development of bioactive molecules and asymmetric synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿10,360.00 |
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| 1g | 10-20 days | ฿45,170.00 |
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| 250mg | 10-20 days | ฿14,000.00 |
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(S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate
Used as a chiral protecting group reagent in organic synthesis, particularly in the preparation of enantiomerically pure compounds. Its main application lies in peptide synthesis and the construction of complex molecules where stereochemical control is critical. The tert-butyl carbamate (Boc) groups provide orthogonal protection for amines, allowing selective deprotection under mild acidic conditions without affecting other sensitive functional groups. The benzyl group can be removed selectively via hydrogenolysis, enabling stepwise assembly of multifunctional molecules. Commonly employed in pharmaceutical research for synthesizing chiral intermediates, especially in the development of bioactive molecules and asymmetric synthesis.
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