(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate
98%
- Product Code: 194757
CAS:
156939-62-7
| Molecular Weight: | 281.31 g./mol | Molecular Formula: | C₁₇H₁₅NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 140-143°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, inert gas atmosphere |
Product Description:
Used primarily as a protected intermediate in peptide synthesis and organic chemistry, particularly in solid-phase synthesis where the (9H-fluoren-9-yl)methoxycarbonyl (Fmoc) group serves as a protecting group for amines. The compound allows for selective deprotection under mild basic conditions, enabling stepwise assembly of peptides without affecting other sensitive functional groups. Its stability under acidic conditions and clean removal with bases like piperidine make it ideal for automated synthesis and the preparation of complex biomolecules. Also employed in the synthesis of specialty polymers and functional materials where controlled reactivity is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿990.00 |
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| 1g | 10-20 days | ฿3,350.00 |
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| 5g | 10-20 days | ฿8,140.00 |
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| 10g | 10-20 days | ฿16,180.00 |
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| 25g | 10-20 days | ฿40,000.00 |
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(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamate
Used primarily as a protected intermediate in peptide synthesis and organic chemistry, particularly in solid-phase synthesis where the (9H-fluoren-9-yl)methoxycarbonyl (Fmoc) group serves as a protecting group for amines. The compound allows for selective deprotection under mild basic conditions, enabling stepwise assembly of peptides without affecting other sensitive functional groups. Its stability under acidic conditions and clean removal with bases like piperidine make it ideal for automated synthesis and the preparation of complex biomolecules. Also employed in the synthesis of specialty polymers and functional materials where controlled reactivity is required.
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