3-Chloro-N-hydroxy-4-methylbenzimidamide

95%

Reagent Code: #163363
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CAS Number 500024-78-2

science Other reagents with same CAS 500024-78-2

blur_circular Chemical Specifications

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Weight 184.62 g/mol
Formula C₈H₉ClN₂O
badge Registry Numbers
MDL Number MFCD05662901
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures. Commonly employed in research settings for structure-activity relationship (SAR) studies, especially in optimizing lead compounds for improved biological activity and selectivity. Also utilized in the preparation of bioactive molecules targeting neurological and oncological pathways.

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inventory 250mg
10-20 days ฿9,630.00

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3-Chloro-N-hydroxy-4-methylbenzimidamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures. Commonly employed in research settings for structure-activity relationship (SAR) studies, especially in optimizing lead compounds for improved biological activity and selectivity. Also utilized in the preparation of bioactive molecules targeting n
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures. Commonly employed in research settings for structure-activity relationship (SAR) studies, especially in optimizing lead compounds for improved biological activity and selectivity. Also utilized in the preparation of bioactive molecules targeting neurological and oncological pathways.
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