2-(Cyanomethyl)-5-hydroxybenzimidazole

≥95%

Reagent Code: #166096
fingerprint
CAS Number 1522542-95-5

science Other reagents with same CAS 1522542-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.17 g/mol
Formula C₉H₇N₃O
badge Registry Numbers
MDL Number MFCD24107454
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of bioactive molecules due to the presence of both cyanomethyl and hydroxybenzimidazole functional groups. Commonly employed in research settings to design compounds with enzyme inhibitory activity. Also utilized in the preparation of fluorescent probes for biochemical assays, leveraging its ability to participate in hydrogen bonding and aromatic interactions. Shows potential in materials science for developing heterocyclic polymers with thermal stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,220.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(Cyanomethyl)-5-hydroxybenzimidazole
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of bioactive molecules due to the presence of both cyanomethyl and hydroxybenzimidazole functional groups. Commonly employed in research settings to design compounds with enzyme inhibitory activity. Also utilized in the preparation of fluorescent probes for biochemical assays, leveraging its ability to participate in hydrogen bonding and aro

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of bioactive molecules due to the presence of both cyanomethyl and hydroxybenzimidazole functional groups. Commonly employed in research settings to design compounds with enzyme inhibitory activity. Also utilized in the preparation of fluorescent probes for biochemical assays, leveraging its ability to participate in hydrogen bonding and aromatic interactions. Shows potential in materials science for developing heterocyclic polymers with thermal stability.

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...