4-Chloro-2-(dimethylamino)nicotinaldehyde

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Reagent Code: #47077
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CAS Number 1160474-84-9

science Other reagents with same CAS 1160474-84-9

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Weight 184.6300 g/mol
Formula C₈H₉ClN₂O
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MDL Number MFCD12025925
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, particularly those targeting neurological and cardiovascular disorders. Its structure allows for the development of complex molecules through reactions like condensation and cyclization. Additionally, it is employed in the synthesis of agrochemicals, contributing to the creation of pesticides and herbicides. Its versatility in forming nitrogen-containing heterocycles makes it valuable in research and industrial applications for designing novel compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,125.00

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4-Chloro-2-(dimethylamino)nicotinaldehyde
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, particularly those targeting neurological and cardiovascular disorders. Its structure allows for the development of complex molecules through reactions like condensation and cyclization. Additionally, it is employed in the synthesis of agrochemicals, contributing to the creation of pesticides and herbicides. Its versatility in forming nitrogen-containing heterocycles makes it valu

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, particularly those targeting neurological and cardiovascular disorders. Its structure allows for the development of complex molecules through reactions like condensation and cyclization. Additionally, it is employed in the synthesis of agrochemicals, contributing to the creation of pesticides and herbicides. Its versatility in forming nitrogen-containing heterocycles makes it valuable in research and industrial applications for designing novel compounds with potential biological activity.

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