Methyl 4-ethyl-3-iodobenzoate

98%

Reagent Code: #206672
fingerprint
CAS Number 51885-91-7

science Other reagents with same CAS 51885-91-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.1 g/mol
Formula C₁₀H₁₁IO₂
thermostat Physical Properties
Boiling Point 326.914°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in functional group transformations. Commonly employed in the development of bioactive molecules where an ethyl-substituted aromatic scaffold is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿900.00
inventory 100mg
10-20 days ฿3,110.00
inventory 250mg
10-20 days ฿5,330.00
inventory 1g
10-20 days ฿14,400.00
inventory 5g
10-20 days ฿35,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 4-ethyl-3-iodobenzoate
No image available
Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in functional group transformations. Commonly employed in the development of bioactive molecules where an ethyl-substituted aromatic scaffold is required.
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...