Acetic acid, (2-pyridinylthio)-, ethyl ester (9CI)

≥95%

Reagent Code: #137465
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CAS Number 28856-92-0

science Other reagents with same CAS 28856-92-0

blur_circular Chemical Specifications

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Weight 197.25 g/mol
Formula C₉H₁₁NO₂S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules where the pyridinylthio group acts as a directing or activating moiety in organic transformations. Commonly employed in the development of herbicides and fungicides due to the bioactive nature of the pyridine ring. Also serves as a reagent in the preparation of thioether-containing compounds with potential medicinal properties. Its ester functionality enables easy modification under mild reaction conditions, making it valuable in research laboratories for building sulfur-linked heterocyclic systems.

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inventory 1g
10-20 days ฿19,650.00

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Acetic acid, (2-pyridinylthio)-, ethyl ester (9CI)
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules where the pyridinylthio group acts as a directing or activating moiety in organic transformations. Commonly employed in the development of herbicides and fungicides due to the bioactive nature of the pyridine ring. Also serves as a reagent in the preparation of thioether-containing compounds with potential medicinal properties. Its ester functionality en
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for incorporation into more complex molecules where the pyridinylthio group acts as a directing or activating moiety in organic transformations. Commonly employed in the development of herbicides and fungicides due to the bioactive nature of the pyridine ring. Also serves as a reagent in the preparation of thioether-containing compounds with potential medicinal properties. Its ester functionality enables easy modification under mild reaction conditions, making it valuable in research laboratories for building sulfur-linked heterocyclic systems.
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