4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde

98%

Reagent Code: #200264
fingerprint
CAS Number 959986-66-4

science Other reagents with same CAS 959986-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.01 g/mol
Formula C₅H₅IN₂O
badge Registry Numbers
MDL Number MFCD22200307
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole scaffolds. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in the design of functional materials and ligands for catalysis due to its reactive aldehyde and halogen groups.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿2,330.00
inventory 1g
10-20 days ฿7,010.00
inventory 5g
10-20 days ฿30,380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole scaffolds. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in the design of functional materials a

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with pyrazole scaffolds. Its iodine functionality allows for further transformations via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for the preparation of kinase inhibitors and other targeted therapies. Also utilized in the design of functional materials and ligands for catalysis due to its reactive aldehyde and halogen groups.

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...