tert-Butyl 4-(3-iodobenzoyl)piperazine-1-carboxylate

98%

Reagent Code: #46239
fingerprint
CAS Number 838845-52-6

science Other reagents with same CAS 838845-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.2540 g/mol
Formula C₁₆H₂₁IN₂O₃
badge Registry Numbers
MDL Number MFCD14635742
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in pharmaceutical research, particularly in the synthesis of compounds with potential therapeutic properties. The presence of the iodobenzoyl group makes it a valuable intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating diverse organic structures. Additionally, the tert-butyl carboxylate group provides stability and can be selectively removed or modified, allowing for further functionalization in multi-step synthetic pathways. Its application is significant in the design and discovery of new drugs, especially in the field of medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,341.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 4-(3-iodobenzoyl)piperazine-1-carboxylate
No image available

This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in pharmaceutical research, particularly in the synthesis of compounds with potential therapeutic properties. The presence of the iodobenzoyl group makes it a valuable intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating diverse organic structures. Additionally, the tert-butyl carboxylate group provi

This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in pharmaceutical research, particularly in the synthesis of compounds with potential therapeutic properties. The presence of the iodobenzoyl group makes it a valuable intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating diverse organic structures. Additionally, the tert-butyl carboxylate group provides stability and can be selectively removed or modified, allowing for further functionalization in multi-step synthetic pathways. Its application is significant in the design and discovery of new drugs, especially in the field of medicinal chemistry.

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...