tert-Butyl 3-iodo-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate

98%

Reagent Code: #118219
fingerprint
CAS Number 657428-43-8

science Other reagents with same CAS 657428-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.14 g/mol
Formula C₁₀H₁₄IN₃O₂
badge Registry Numbers
MDL Number MFCD28404922
inventory_2 Storage & Handling
Storage 2-8°C, protected from light

description Product Description

This chemical is primarily utilized in organic synthesis, particularly as a versatile intermediate in the development of pharmaceutical compounds. Its structure, featuring both an iodo group and a protected amine, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions enable the creation of complex molecules, often targeting biologically active compounds or drug candidates. Additionally, the tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating the synthesis of pyrrolopyrazole derivatives, which are common scaffolds in medicinal chemistry. Its applications are particularly relevant in the design of kinase inhibitors and other therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,665.00
inventory 100mg
10-20 days ฿17,136.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 3-iodo-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate
No image available

This chemical is primarily utilized in organic synthesis, particularly as a versatile intermediate in the development of pharmaceutical compounds. Its structure, featuring both an iodo group and a protected amine, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions enable the creation of complex molecules, often targeting biologically active compounds or drug candidates. Additionally, the tert-butyloxycarbonyl (Boc) pr

This chemical is primarily utilized in organic synthesis, particularly as a versatile intermediate in the development of pharmaceutical compounds. Its structure, featuring both an iodo group and a protected amine, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions enable the creation of complex molecules, often targeting biologically active compounds or drug candidates. Additionally, the tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating the synthesis of pyrrolopyrazole derivatives, which are common scaffolds in medicinal chemistry. Its applications are particularly relevant in the design of kinase inhibitors and other therapeutic agents.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...