Methyl 2-bromo-4-methylthiazole-5-carboxylate

96%

Reagent Code: #43249
fingerprint
CAS Number 81569-51-9

science Other reagents with same CAS 81569-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.0863 g/mol
Formula C₆H₆BrNO₂S
badge Registry Numbers
MDL Number MFCD09998944
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a carboxylate ester group, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other biologically active compounds. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce thiazole moieties into target molecules. Additionally, it serves as a precursor in the synthesis of thiazole-containing heterocycles, which are common in drug discovery due to their diverse pharmacological properties. Its reactivity and functional groups allow for further derivatization, enabling the creation of tailored compounds for specific applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,682.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 2-bromo-4-methylthiazole-5-carboxylate
No image available

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a carboxylate ester group, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other biologically active compounds. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce thiazole moieties into target molecules. Additionally

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom and a carboxylate ester group, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other biologically active compounds. Specifically, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce thiazole moieties into target molecules. Additionally, it serves as a precursor in the synthesis of thiazole-containing heterocycles, which are common in drug discovery due to their diverse pharmacological properties. Its reactivity and functional groups allow for further derivatization, enabling the creation of tailored compounds for specific applications.

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...