(9H-fluoren-9-yl)methyl3-aminophenylcarbamate
98%
- Product Code: 37143
CAS:
1629477-47-9
| Molecular Weight: | 330.38 g./mol | Molecular Formula: | C₂₁H₁₈N₂O₂ |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in the field of organic synthesis and peptide chemistry as a protecting group for amines. It is particularly valuable in solid-phase peptide synthesis (SPPS) where it helps to protect the amine functional group during the assembly of peptide chains. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, can be selectively removed under mild basic conditions, allowing for the stepwise construction of peptides without affecting other sensitive functional groups. Additionally, it is employed in the preparation of various pharmaceutical intermediates and bioactive molecules, where selective protection and deprotection of amines are crucial for achieving the desired chemical transformations. Its stability under acidic conditions and ease of removal make it a versatile tool in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿43,200.00 |
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(9H-fluoren-9-yl)methyl3-aminophenylcarbamate
This chemical is primarily used in the field of organic synthesis and peptide chemistry as a protecting group for amines. It is particularly valuable in solid-phase peptide synthesis (SPPS) where it helps to protect the amine functional group during the assembly of peptide chains. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, can be selectively removed under mild basic conditions, allowing for the stepwise construction of peptides without affecting other sensitive functional groups. Additionally, it is employed in the preparation of various pharmaceutical intermediates and bioactive molecules, where selective protection and deprotection of amines are crucial for achieving the desired chemical transformations. Its stability under acidic conditions and ease of removal make it a versatile tool in synthetic organic chemistry.
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