3,5-Dichloro-2-isopropoxypyridine

95%

Reagent Code: #178414
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CAS Number 1394964-34-1

science Other reagents with same CAS 1394964-34-1

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Storage 2-8°C, dry

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Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific plant enzymes or insect nervous systems, enhancing selectivity and efficacy. Also utilized in the production of pharmaceuticals where chlorinated pyridine derivatives contribute to bioactive molecule design. The isopropoxy group aids in improving lipophilicity, which can enhance membrane permeability in crop protection agents. Commonly employed in research and development for new agrochemical formulations due to its reactivity and stability in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,920.00

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3,5-Dichloro-2-isopropoxypyridine
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Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific plant enzymes or insect nervous systems, enhancing selectivity and efficacy. Also utilized in the production of pharmaceuticals where chlorinated pyridine derivatives contribute to bioactive molecule design. The isopropoxy group aids in improving lipophilicity, which can enhance membrane permeability in crop prot

Used as a key intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. Its structure supports the development of active ingredients that target specific plant enzymes or insect nervous systems, enhancing selectivity and efficacy. Also utilized in the production of pharmaceuticals where chlorinated pyridine derivatives contribute to bioactive molecule design. The isopropoxy group aids in improving lipophilicity, which can enhance membrane permeability in crop protection agents. Commonly employed in research and development for new agrochemical formulations due to its reactivity and stability in multi-step syntheses.

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