(6-((tert-Butoxycarbonyl)amino)naphthalen-2-yl)boronic acid

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Reagent Code: #129865
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CAS Number 1131395-21-5

science Other reagents with same CAS 1131395-21-5

blur_circular Chemical Specifications

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Weight 287.12 g/mol
Formula C₁₅H₁₈BNO₄
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MDL Number MFCD24470899
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for the construction of complex aromatic frameworks in drug discovery. The Boc-protected amine provides stability and selective deprotection for further functionalization, making it valuable in multi-step organic syntheses. Commonly employed in research settings for creating targeted libraries of compounds in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,300.00
inventory 250mg
10-20 days ฿4,990.00

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(6-((tert-Butoxycarbonyl)amino)naphthalen-2-yl)boronic acid
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for the construction of complex aromatic frameworks in drug discovery. The Boc-protected amine provides stability and selective deprotection for further functionalization, making it valuable in multi-step organic syntheses. Commonly employed in research settings for creating targeted libr

Used as an intermediate in pharmaceutical synthesis, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing for the construction of complex aromatic frameworks in drug discovery. The Boc-protected amine provides stability and selective deprotection for further functionalization, making it valuable in multi-step organic syntheses. Commonly employed in research settings for creating targeted libraries of compounds in medicinal chemistry.

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