Tert-butyl 2-(chloromethyl)-1H-benzo[d]imidazole-1-carboxylate

≥95%

Reagent Code: #240207
fingerprint
CAS Number 163798-87-6

science Other reagents with same CAS 163798-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.73 g/mol
Formula C₁₃H₁₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD10697638
inventory_2 Storage & Handling
Density 1.23±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 antiviral and antifungal agents. Its structure allows for easy modification of the benzimidazole core, making it valuable in medicinal chemistry for creating compounds with enhanced biological activity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the reactivity of the chloromethyl group, which can be further substituted to introduce various functional moieties. Also utilized in agrochemical research for designing new active ingredients in crop protection agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,320.00
inventory 5g
10-20 days ฿18,410.00
inventory 100mg
10-20 days ฿1,570.00
inventory 1g
10-20 days ฿4,870.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-butyl 2-(chloromethyl)-1H-benzo[d]imidazole-1-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antifungal agents. Its structure allows for easy modification of the benzimidazole core, making it valuable in medicinal chemistry for creating compounds with enhanced biological activity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the reactivity of the chloromethyl group, which can be further substituted to introduce various functional moieties. Also

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antifungal agents. Its structure allows for easy modification of the benzimidazole core, making it valuable in medicinal chemistry for creating compounds with enhanced biological activity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the reactivity of the chloromethyl group, which can be further substituted to introduce various functional moieties. Also utilized in agrochemical research for designing new active ingredients in crop protection agents.

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...