6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester

96%

Reagent Code: #49910
fingerprint
CAS Number 1402666-66-3

science Other reagents with same CAS 1402666-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.0586 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD26517010
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine moiety into target compounds. Additionally, it serves as a precursor in the preparation of agrochemicals and fine chemicals, where the pyridine ring plays a crucial role in the biological activity of the final product. Its ester group can also be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,082.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester
No image available

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine moiety into target compounds. Additionally, it serves as

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyridine moiety into target compounds. Additionally, it serves as a precursor in the preparation of agrochemicals and fine chemicals, where the pyridine ring plays a crucial role in the biological activity of the final product. Its ester group can also be hydrolyzed or transformed into other functional groups, further expanding its utility in synthetic 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...