4-Iodo-1-trityl-1H-pyrazole

≥95%

Reagent Code: #119536
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CAS Number 191980-54-8

science Other reagents with same CAS 191980-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.29 g/mol
Formula C₂₂H₁₇IN₂
badge Registry Numbers
MDL Number MFCD23135653
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed away from light

description Product Description

This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, particularly in the synthesis of pyrazole derivatives, which are known for their biological activities. The trityl group provides protection for the nitrogen atom during reactions, allowing for selective modifications at other positions of the pyrazole ring. Additionally, the iodine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse compounds for drug discovery and material science applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿783.00
inventory 1g
10-20 days ฿2,322.00
inventory 100mg
10-20 days ฿468.00

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4-Iodo-1-trityl-1H-pyrazole
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This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, particularly in the synthesis of pyrazole derivatives, which are known for their biological activities. The trityl group provides protection for the nitrogen atom during reactions, allowing for selective modifications at other positions of the pyrazole ring. Additionally, the iodine atom offers a reactive site fo

This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, particularly in the synthesis of pyrazole derivatives, which are known for their biological activities. The trityl group provides protection for the nitrogen atom during reactions, allowing for selective modifications at other positions of the pyrazole ring. Additionally, the iodine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse compounds for drug discovery and material science applications.

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