N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide

99%

Reagent Code: #216860
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CAS Number 4433-79-8

science Other reagents with same CAS 4433-79-8

blur_circular Chemical Specifications

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Weight 271.70 g/mol
Formula C₁₂H₁₄ClNO₄
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MDL Number MFCD00026256
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Used primarily in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure supports the development of bioactive molecules, particularly in the design of compounds with central nervous system activity. Commonly employed in the preparation of substituted phenylacetamides and related derivatives showing potential anticonvulsant or analgesic properties. Also utilized in research settings for structure-activity relationship (SAR) studies due to its functional groups that allow further chemical modifications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿138.00
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿770.00
inventory 100g
10-20 days ฿1,507.00
inventory 500g
10-20 days ฿13,640.00

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N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide
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Used primarily in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure supports the development of bioactive molecules, particularly in the design of compounds with central nervous system activity. Commonly employed in the preparation of substituted phenylacetamides and related derivatives showing potential anticonvulsant or analgesic properties. Also utilized in research settings for structure-activity relationship (SAR) studies due to its functional groups that allo

Used primarily in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure supports the development of bioactive molecules, particularly in the design of compounds with central nervous system activity. Commonly employed in the preparation of substituted phenylacetamides and related derivatives showing potential anticonvulsant or analgesic properties. Also utilized in research settings for structure-activity relationship (SAR) studies due to its functional groups that allow further chemical modifications.

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