2-(BROMOMETHYL)-1-METHYL-1H-BENZIMIDAZOLE HBR

95%

Reagent Code: #156340
fingerprint
CAS Number 934570-40-8

science Other reagents with same CAS 934570-40-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.00 g/mol
Formula C₉H₁₀Br₂N₂
badge Registry Numbers
MDL Number MFCD09702343
thermostat Physical Properties
Melting Point >170 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It plays a key role in creating compounds with antiparasitic, antiviral, and anticancer activities. Its reactive bromomethyl group allows for easy alkylation, making it valuable in constructing complex molecules in medicinal chemistry. Commonly employed in research settings to develop proton pump inhibitors and anthelmintic agents. Also utilized in the preparation of functionalized benzimidazole derivatives for use in agrochemicals and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,100.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(BROMOMETHYL)-1-METHYL-1H-BENZIMIDAZOLE HBR
No image available

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It plays a key role in creating compounds with antiparasitic, antiviral, and anticancer activities. Its reactive bromomethyl group allows for easy alkylation, making it valuable in constructing complex molecules in medicinal chemistry. Commonly employed in research settings to develop proton pump inhibitors and anthelmintic agents. Also utilized in the preparation of functi

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It plays a key role in creating compounds with antiparasitic, antiviral, and anticancer activities. Its reactive bromomethyl group allows for easy alkylation, making it valuable in constructing complex molecules in medicinal chemistry. Commonly employed in research settings to develop proton pump inhibitors and anthelmintic agents. Also utilized in the preparation of functionalized benzimidazole derivatives for use in agrochemicals and materials science.

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...