tert-Butyl 7-bromo-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate
97%
- Product Code: 149802
CAS:
886364-30-3
| Molecular Weight: | 327.22 g./mol | Molecular Formula: | C₁₄H₁₉BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07369867 | |
| Melting Point: | Boiling Point: | 420°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the construction of benzodiazepine-like frameworks, which are commonly found in anxiolytic, anticonvulsant, and sedative drugs. The bromo functional group allows for further cross-coupling reactions, enabling the introduction of diverse substituents during drug optimization. The tert-butyl carboxylate group acts as a protected amine, facilitating selective deprotection and derivatization in multistep synthetic routes. Widely employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿23,220.00 |
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tert-Butyl 7-bromo-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the construction of benzodiazepine-like frameworks, which are commonly found in anxiolytic, anticonvulsant, and sedative drugs. The bromo functional group allows for further cross-coupling reactions, enabling the introduction of diverse substituents during drug optimization. The tert-butyl carboxylate group acts as a protected amine, facilitating selective deprotection and derivatization in multistep synthetic routes. Widely employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.
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