ethyl 3-(1-methyl-1H-pyrazol-4-yl)propanoate

95%

Reagent Code: #196466
fingerprint
CAS Number 192661-37-3

science Other reagents with same CAS 192661-37-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.22 g/mol
Formula C₉H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD21642848
thermostat Physical Properties
Boiling Point 274.2±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients targeting central nervous system disorders and inflammation. Its structure allows for easy modification, making it valuable in medicinal chemistry for creating novel pyrazole-based compounds. Also employed in agrochemical research for designing new pesticides and herbicides due to the bioactive nature of pyrazole derivatives. Commonly utilized in organic synthesis to build more complex molecules through ester hydrolysis, coupling reactions, or heterocyclic elaboration.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,780.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
ethyl 3-(1-methyl-1H-pyrazol-4-yl)propanoate
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients targeting central nervous system disorders and inflammation. Its structure allows for easy modification, making it valuable in medicinal chemistry for creating novel pyrazole-based compounds. Also employed in agrochemical research for designing new pesticides and herbicides due to the bioactive nature of pyrazole derivatives. Commonly utilized in organic synthesis to build more complex molec

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients targeting central nervous system disorders and inflammation. Its structure allows for easy modification, making it valuable in medicinal chemistry for creating novel pyrazole-based compounds. Also employed in agrochemical research for designing new pesticides and herbicides due to the bioactive nature of pyrazole derivatives. Commonly utilized in organic synthesis to build more complex molecules through ester hydrolysis, coupling reactions, or heterocyclic elaboration.

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...