tert-Butyl 3-bromo-5,6-dihydroimidazo[1,5-a]pyrazine-7(8H)-carboxylate

≥95%

Reagent Code: #45251
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CAS Number 1188264-74-5

science Other reagents with same CAS 1188264-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.17 g/mol
Formula C₁₁H₁₆BrN₃O₂
badge Registry Numbers
MDL Number MFCD13152219
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the development of pharmaceutical agents. It is particularly valuable in the construction of complex heterocyclic structures, which are often found in bioactive molecules. Its bromo and carboxylate functional groups enable it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the creation of diverse chemical libraries for drug discovery. Additionally, its tert-butyl protecting group enhances stability during synthetic processes, making it a versatile building block in medicinal chemistry.

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Test Parameter Specification
Appearance White to Off White Solid
Purity (%) 95-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿63,180.00
inventory 1g
10-20 days ฿35,460.00
inventory 250mg
10-20 days ฿13,140.00
inventory 100mg
10-20 days ฿7,730.00

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tert-Butyl 3-bromo-5,6-dihydroimidazo[1,5-a]pyrazine-7(8H)-carboxylate
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This compound is primarily utilized in organic synthesis as a key intermediate for the development of pharmaceutical agents. It is particularly valuable in the construction of complex heterocyclic structures, which are often found in bioactive molecules. Its bromo and carboxylate functional groups enable it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the creation of diverse chemical libraries for drug discovery. Additionally, its tert-butyl pro

This compound is primarily utilized in organic synthesis as a key intermediate for the development of pharmaceutical agents. It is particularly valuable in the construction of complex heterocyclic structures, which are often found in bioactive molecules. Its bromo and carboxylate functional groups enable it to participate in various coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, facilitating the creation of diverse chemical libraries for drug discovery. Additionally, its tert-butyl protecting group enhances stability during synthetic processes, making it a versatile building block in medicinal chemistry.

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