6-Bromo-2-chloronicotinaldehyde

98%

Reagent Code: #148364
fingerprint
CAS Number 1125410-08-3

science Other reagents with same CAS 1125410-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.45 g/mol
Formula C₆H₃BrClNO
badge Registry Numbers
MDL Number MFCD11857709
thermostat Physical Properties
Boiling Point 310°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and agrochemicals. Its functional groups enable selective reactions for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it plays a role in creating active ingredients in crop protection agents and central nervous system therapeutics. Its aldehyde group allows for further derivatization, making it valuable in medicinal chemistry for lead optimization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,810.00
inventory 250mg
10-20 days ฿6,450.00
inventory 1g
10-20 days ฿16,820.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-2-chloronicotinaldehyde
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and agrochemicals. Its functional groups enable selective reactions for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it plays a role in creating active ingredients in crop protection agents and central nervous system therapeutics. Its aldehyde group allows for further derivatization, making it valuable i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and agrochemicals. Its functional groups enable selective reactions for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it plays a role in creating active ingredients in crop protection agents and central nervous system therapeutics. Its aldehyde group allows for further derivatization, making it valuable in medicinal chemistry for lead optimization.

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...