2-bromo-4-fluoro-5-methylbenzonitrile

98%

Reagent Code: #144213
fingerprint
CAS Number 916792-07-9

science Other reagents with same CAS 916792-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.03 g/mol
Formula C₈H₅BrFN
badge Registry Numbers
MDL Number MFCD07782070
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build biaryl or aryl amine systems. Also utilized in the preparation of kinase inhibitors and other biologically active compounds due to the presence of halogen and nitrile groups that serve as reaction handles. Its versatility supports applications in drug discovery and process chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white to light brown solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿319.00
inventory 5g
10-20 days ฿731.50
inventory 25g
10-20 days ฿6,490.00
inventory 100g
10-20 days ฿25,300.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-bromo-4-fluoro-5-methylbenzonitrile
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build biaryl or aryl amine systems. Also utilized in the preparation of kinase inhibitors and other biologically active

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build biaryl or aryl amine systems. Also utilized in the preparation of kinase inhibitors and other biologically active compounds due to the presence of halogen and nitrile groups that serve as reaction handles. Its versatility supports applications in drug discovery and process chemistry.

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...