2-bromo-6-methylpyridine-3-carbonitrile

≥95%

Reagent Code: #144118
fingerprint
CAS Number 155265-57-9

science Other reagents with same CAS 155265-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
badge Registry Numbers
MDL Number MFCD06254423
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 kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new pesticides and herbicides due to its ability to enhance binding affinity and metabolic stability in target molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,050.00
inventory 250mg
10-20 days ฿3,420.00
inventory 1g
10-20 days ฿8,200.00
inventory 5g
10-20 days ฿35,530.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-bromo-6-methylpyridine-3-carbonitrile
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new pesticides and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new pesticides and herbicides due to its ability to enhance binding affinity and metabolic stability in target 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...