1H-Benzimidazole-5-carbaldehyde

≥97%

Reagent Code: #172889
fingerprint
CAS Number 58442-17-4

science Other reagents with same CAS 58442-17-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.15 g/mol
Formula C₈H₆N₂O
badge Registry Numbers
MDL Number MFCD08741423
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its aldehyde functional group allows for easy modification, enabling the formation of Schiff bases and other derivatives important in drug design. Commonly employed in the preparation of benzimidazole-based compounds that exhibit biological activity, including kinase inhibitors and antimicrobial agents. Also utilized in the creation of fluorescent probes and sensors due to its ability to form conjugated systems useful in imaging and diagnostic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿4,690.00
inventory 5g
10-20 days ฿21,570.00
inventory 250mg
10-20 days ฿1,970.00
inventory 10g
10-20 days ฿42,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1H-Benzimidazole-5-carbaldehyde
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its aldehyde functional group allows for easy modification, enabling the formation of Schiff bases and other derivatives important in drug design. Commonly employed in the preparation of benzimidazole-based compounds that exhibit biological activity, including kinase inhibitors and antimicrobial agents. Also utilized in the creation of fluorescent probes and sensors due t

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its aldehyde functional group allows for easy modification, enabling the formation of Schiff bases and other derivatives important in drug design. Commonly employed in the preparation of benzimidazole-based compounds that exhibit biological activity, including kinase inhibitors and antimicrobial agents. Also utilized in the creation of fluorescent probes and sensors due to its ability to form conjugated systems useful in imaging and diagnostic applications.

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...