3-Fluoro-5-methylisonicotinic acid hydrochloride

97%

Reagent Code: #130641
fingerprint
CAS Number 2639626-30-3

science Other reagents with same CAS 2639626-30-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.59 g/mol
Formula C₇H₇ClFNO₂
badge Registry Numbers
MDL Number MFCD33395925
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom and the carboxylic acid functionality, which allows for easy derivatization into amides and esters. Also utilized in the preparation of nicotinic acid analogs with potential neurological or anti-inflammatory activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,100.00
inventory 250mg
10-20 days ฿6,960.00
inventory 1g
10-20 days ฿20,340.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Fluoro-5-methylisonicotinic acid hydrochloride
No image available

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom and the carboxylic acid functionality, which allows for easy derivatization into amides and esters. Also utilized in

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom and the carboxylic acid functionality, which allows for easy derivatization into amides and esters. Also utilized in the preparation of nicotinic acid analogs with potential neurological or anti-inflammatory activity.

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...