3-Bromo-2-chloro-4-methyl-5-nitropyridine

97%

Reagent Code: #151222
fingerprint
CAS Number 1049706-73-1

science Other reagents with same CAS 1049706-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.47 g/mol
Formula C₆H₄BrClN₂O₂
badge Registry Numbers
MDL Number MFCD12024452
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen and nitro functional groups allow for selective substitution reactions, making it valuable in building complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of bioactive compounds with potential antimicrobial or insecticidal properties. Its reactivity profile supports use in research and development of novel active ingredients in crop protection and medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿590.00
inventory 250mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿3,980.00
inventory 5g
10-20 days ฿13,950.00
inventory 25g
10-20 days ฿63,980.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Bromo-2-chloro-4-methyl-5-nitropyridine
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen and nitro functional groups allow for selective substitution reactions, making it valuable in building complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of bioactive compounds with potential antimicrobial or inse

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen and nitro functional groups allow for selective substitution reactions, making it valuable in building complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of bioactive compounds with potential antimicrobial or insecticidal properties. Its reactivity profile supports use in research and development of novel active ingredients in crop protection and medicinal 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...