5-Bromo-2-chloro-4-methylpyridin-3-amine

98%

Reagent Code: #148354
fingerprint
CAS Number 1204231-59-3

science Other reagents with same CAS 1204231-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.48 g/mol
Formula C₆H₆BrClN₂
badge Registry Numbers
MDL Number MFCD16170477
thermostat Physical Properties
Boiling Point 316.4±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its halogenated pyridine structure, which enhances bioactivity. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in drug discovery and material science. Its amine group allows for easy coupling reactions, making it valuable in combinatorial chemistry and the design of biologically active molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,130.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-2-chloro-4-methylpyridin-3-amine
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its halogenated pyridine structure, which enhances bioactivity. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in drug discovery and material science. Its amine group allows for easy coupling reactions, making

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its halogenated pyridine structure, which enhances bioactivity. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in drug discovery and material science. Its amine group allows for easy coupling reactions, making it valuable in combinatorial chemistry and the design of biologically active molecules.

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...