(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)boronic acid

97%

Reagent Code: #91038
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CAS Number 844501-00-4

science Other reagents with same CAS 844501-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.07 g/mol
Formula C₁₀H₁₈BNO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and facilitates selective reactions, making it a versatile building block in multi-step synthetic processes. Its applications extend to the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases.

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Test Parameter Specification
APPEARANCE White to Off-white to Pale yellow to Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿675.00
inventory 100mg
10-20 days ฿1,440.00
inventory 250mg
10-20 days ฿3,222.00
inventory 1g
10-20 days ฿9,090.00
inventory 5g
10-20 days ฿41,400.00

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(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enha

This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and facilitates selective reactions, making it a versatile building block in multi-step synthetic processes. Its applications extend to the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases.

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