Ethyl 1-benzyl-4-bromo-5-methyl-1H-pyrazole-3-carboxylate

95%

Reagent Code: #184996
fingerprint
CAS Number 1262415-66-6

science Other reagents with same CAS 1262415-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.19 g/mol
Formula C₁₄H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD19443879
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. It is also employed in research settings to design biologically active molecules targeting central nervous system disorders and metabolic diseases. The bromo and ester groups enable cross-coupling reactions and nucleophilic substitutions, facilitating the creation of diverse compound libraries for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,940.00
inventory 250mg
10-20 days ฿18,320.00
inventory 1g
10-20 days ฿55,490.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 1-benzyl-4-bromo-5-methyl-1H-pyrazole-3-carboxylate
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. It is also employed in research settings to design biologically active molecules targeting central nervous system disorders and metabolic diseases. The bromo and ester groups enable cross-coupling reactions and nucleop

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing pyrazole-based drug candidates. It is also employed in research settings to design biologically active molecules targeting central nervous system disorders and metabolic diseases. The bromo and ester groups enable cross-coupling reactions and nucleophilic substitutions, facilitating the creation of diverse compound libraries for drug discovery.

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...