Isoxazol-3-ylmethanol

98%

Reagent Code: #199712
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CAS Number 89102-73-8

science Other reagents with same CAS 89102-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 99.09 g/mol
Formula C₄H₅NO₂
badge Registry Numbers
MDL Number MFCD07778413
thermostat Physical Properties
Boiling Point 240°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of β-lactam antibiotics and other biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building heterocyclic scaffolds. It is also employed in the development of agrochemicals and as a building block in combinatorial chemistry for drug discovery. The hydroxyl group enables easy derivatization, such as esterification or ether formation, while the isoxazole ring contributes metabolic stability and polarity to final products.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿520.00
250mg
10-20 days ฿1,550.00
1g
10-20 days ฿3,540.00
Isoxazol-3-ylmethanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of β-lactam antibiotics and other biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building heterocyclic scaffolds. It is also employed in the development of agrochemicals and as a building block in combinatorial chemistry for drug discovery. The hydroxyl group enables easy derivatization, such as esterification or ether for
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of β-lactam antibiotics and other biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building heterocyclic scaffolds. It is also employed in the development of agrochemicals and as a building block in combinatorial chemistry for drug discovery. The hydroxyl group enables easy derivatization, such as esterification or ether formation, while the isoxazole ring contributes metabolic stability and polarity to final products.
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