tert-Butyl 6-nitro-3,4-dihydroisoquinoline-2(1H)-carboxylate

97%

Reagent Code: #148499
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CAS Number 186390-79-4

science Other reagents with same CAS 186390-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.30 g/mol
Formula C₁₄H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD09864789
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing isoquinoline-based molecules, which are commonly found in central nervous system agents, including potential antidepressants, antipsychotics, and anti-addiction drugs. The nitro group allows for further functionalization, enabling the introduction of amines or other substituents through reduction or substitution reactions. Its protected amine (Boc group) facilitates selective deprotection and coupling in multi-step syntheses, making it valuable in medicinal chemistry for creating novel drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,240.00
250mg
10-20 days ฿2,200.00
1g
10-20 days ฿7,160.00
5g
10-20 days ฿33,510.00
tert-Butyl 6-nitro-3,4-dihydroisoquinoline-2(1H)-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing isoquinoline-based molecules, which are commonly found in central nervous system agents, including potential antidepressants, antipsychotics, and anti-addiction drugs. The nitro group allows for further functionalization, enabling the introduction of amines or other substituents through reduction or substitution reactions. Its protected amine (Bo

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing isoquinoline-based molecules, which are commonly found in central nervous system agents, including potential antidepressants, antipsychotics, and anti-addiction drugs. The nitro group allows for further functionalization, enabling the introduction of amines or other substituents through reduction or substitution reactions. Its protected amine (Boc group) facilitates selective deprotection and coupling in multi-step syntheses, making it valuable in medicinal chemistry for creating novel drug candidates.

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