3-Iodo-1,4-dimethyl-1H-pyrazole

≥95%

Reagent Code: #200230
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CAS Number 1395443-04-5

science Other reagents with same CAS 1395443-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.03 g/mol
Formula C₅H₇IN₂
badge Registry Numbers
MDL Number MFCD23769065
thermostat Physical Properties
Boiling Point 241.5°C at 760 mmHg
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, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced potency and selectivity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing new active ingredients with improved stability and activity profiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,380.00
inventory 250mg
10-20 days ฿5,910.00
inventory 1g
10-20 days ฿20,480.00

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3-Iodo-1,4-dimethyl-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced potency and selectivity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced potency and selectivity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing new active ingredients with improved stability and activity profiles.

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