6-Methyl-2-oxo-2H-pyran-4-yl 4-methylbenzene-1-sulfonate

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Reagent Code: #203909
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CAS Number 31913-41-4

science Other reagents with same CAS 31913-41-4

blur_circular Chemical Specifications

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Weight 280.3 g/mol
Formula C₁₃H₁₂O₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to its reactive ester and lactone functionalities. Commonly employed in the preparation of coumarin derivatives, which exhibit biological activities such as anticoagulant, antimicrobial, and antioxidant properties. Also utilized in research settings for designing enzyme inhibitors and fluorescent probes. Its sulfonate group enhances solubility and reactivity in various coupling reactions, making it valuable in medicinal chemistry and materials science.

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inventory 1g
10-20 days ฿21,000.00

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6-Methyl-2-oxo-2H-pyran-4-yl 4-methylbenzene-1-sulfonate
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to its reactive ester and lactone functionalities. Commonly employed in the preparation of coumarin derivatives, which exhibit biological activities such as anticoagulant, antimicrobial, and antioxidant properties. Also utilized in research settings for designing enzyme inhibitors and fluorescent probes. Its sulfonate

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to its reactive ester and lactone functionalities. Commonly employed in the preparation of coumarin derivatives, which exhibit biological activities such as anticoagulant, antimicrobial, and antioxidant properties. Also utilized in research settings for designing enzyme inhibitors and fluorescent probes. Its sulfonate group enhances solubility and reactivity in various coupling reactions, making it valuable in medicinal chemistry and materials science.

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