(9H-Fluoren-9-yl)methyl (6-hydroxy-5-(hydroxymethyl)hexyl)carbamate
95%
- Product Code: 82913
CAS:
147190-31-6
| Molecular Weight: | 369.45 g./mol | Molecular Formula: | C₂₂H₂₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094253 | |
| Melting Point: | Boiling Point: | 617.0±50.0 °C(Predicted) | |
| Density: | 1.195±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and peptide chemistry as a protective group for amines. Its structure allows it to be selectively attached to amino groups, safeguarding them during complex chemical reactions. Once the desired reactions are complete, it can be removed under mild conditions, making it highly valuable in the synthesis of sensitive compounds like peptides and proteins. Additionally, its stability under various reaction conditions ensures that it does not interfere with other functional groups, making it a versatile tool in the development of pharmaceuticals and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $507.21 |
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| 0.250 | 10-20 days | $887.62 |
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| 1.000 | 10-20 days | $1,785.38 |
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(9H-Fluoren-9-yl)methyl (6-hydroxy-5-(hydroxymethyl)hexyl)carbamate
This chemical is primarily utilized in the field of organic synthesis and peptide chemistry as a protective group for amines. Its structure allows it to be selectively attached to amino groups, safeguarding them during complex chemical reactions. Once the desired reactions are complete, it can be removed under mild conditions, making it highly valuable in the synthesis of sensitive compounds like peptides and proteins. Additionally, its stability under various reaction conditions ensures that it does not interfere with other functional groups, making it a versatile tool in the development of pharmaceuticals and bioactive molecules.
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