Ethyl 1,3-Dithiolane-2-carboxylate

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Reagent Code: #183141
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CAS Number 20461-99-8

science Other reagents with same CAS 20461-99-8

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Weight 178.26 g/mol
Formula C₆H₁₀O₂S₂
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MDL Number MFCD00005411
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Storage Room temperature

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Widely used in organic synthesis as a key intermediate for the preparation of sulfur-containing compounds. It serves as a protecting group for carbonyl functionalities, especially in multistep synthesis of complex molecules like pharmaceuticals and natural products. The dithiolane ring can reversibly form thioacetals with aldehydes and ketones, making it valuable in selective reactions where carbonyl stability is required under basic or nucleophilic conditions. Commonly employed in the synthesis of heterocycles, agrochemicals, and bioactive molecules due to its stability and ease of deprotection under mild acidic conditions. Also utilized in the development of specialty polymers and ligands for metal catalysis.

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inventory 1g
10-20 days ฿1,760.00

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Ethyl 1,3-Dithiolane-2-carboxylate
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Widely used in organic synthesis as a key intermediate for the preparation of sulfur-containing compounds. It serves as a protecting group for carbonyl functionalities, especially in multistep synthesis of complex molecules like pharmaceuticals and natural products. The dithiolane ring can reversibly form thioacetals with aldehydes and ketones, making it valuable in selective reactions where carbonyl stability is required under basic or nucleophilic conditions. Commonly employed in the synthesis of heter

Widely used in organic synthesis as a key intermediate for the preparation of sulfur-containing compounds. It serves as a protecting group for carbonyl functionalities, especially in multistep synthesis of complex molecules like pharmaceuticals and natural products. The dithiolane ring can reversibly form thioacetals with aldehydes and ketones, making it valuable in selective reactions where carbonyl stability is required under basic or nucleophilic conditions. Commonly employed in the synthesis of heterocycles, agrochemicals, and bioactive molecules due to its stability and ease of deprotection under mild acidic conditions. Also utilized in the development of specialty polymers and ligands for metal catalysis.

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