(5-Bromo-4-chloro-2-fluorophenyl)methanol

97%

Reagent Code: #156039
fingerprint
CAS Number 1785275-10-6

science Other reagents with same CAS 1785275-10-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.47 g/mol
Formula C₇H₅BrClFO
badge Registry Numbers
MDL Number MFCD28060809
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its functionalized aromatic structure allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the substituted phenyl ring into larger bioactive structures. Also utilized in the preparation of agrochemicals and specialty materials where halogenated building blocks are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿93,980.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(5-Bromo-4-chloro-2-fluorophenyl)methanol
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its functionalized aromatic structure allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the substituted phenyl ring into larger bioactive structures. Also utilized in the preparation of agrochemicals and special

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its functionalized aromatic structure allows for selective modifications, making it valuable in medicinal chemistry for constructing complex drug molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the substituted phenyl ring into larger bioactive structures. Also utilized in the preparation of agrochemicals and specialty materials where halogenated building blocks are 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...