tert-Butyl 7-bromo-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate

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Reagent Code: #149802
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CAS Number 886364-30-3

science Other reagents with same CAS 886364-30-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.22 g/mol
Formula C₁₄H₁₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD07369867
thermostat Physical Properties
Boiling Point 420°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description 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.

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inventory 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
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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

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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