tert-Butyl 2-amino-1H-benzo[d]imidazole-1-carboxylate
95%
- Product Code: 42519
CAS:
1383133-23-0
| Molecular Weight: | 233.2664 g./mol | Molecular Formula: | C₁₂H₁₅N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22415337 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a protective group for amines, particularly in the preparation of pharmaceuticals and biologically active molecules. Its tert-butyloxycarbonyl (Boc) group effectively shields the amine functionality during multi-step reactions, allowing selective transformations elsewhere in the molecule. It is also employed in the synthesis of benzimidazole derivatives, which are key intermediates in the development of drugs targeting various conditions, including infections, inflammation, and cancer. Additionally, its stability under basic conditions makes it a valuable reagent in peptide chemistry for protecting amino acids during peptide bond formation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $638.27 |
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tert-Butyl 2-amino-1H-benzo[d]imidazole-1-carboxylate
This compound is primarily utilized in organic synthesis as a protective group for amines, particularly in the preparation of pharmaceuticals and biologically active molecules. Its tert-butyloxycarbonyl (Boc) group effectively shields the amine functionality during multi-step reactions, allowing selective transformations elsewhere in the molecule. It is also employed in the synthesis of benzimidazole derivatives, which are key intermediates in the development of drugs targeting various conditions, including infections, inflammation, and cancer. Additionally, its stability under basic conditions makes it a valuable reagent in peptide chemistry for protecting amino acids during peptide bond formation.
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