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78205-18-2

AcetaMide, 2-chloro-N-3-pyridinyl-

Catalog#: AR005P0M  |   CAS#: 78205-18-2  |   MDL#: MFCD00772161  |   MF: C7H7ClN2O  |   MW: 170.5963

Packsize Purity Price Availability Quantity
500mg 97% $121.00 Global Stock Buy Now Add To Cart
1g 97% $180.00 Global Stock Buy Now Add To Cart
5g 97% $543.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005P0M
Chemical Name AcetaMide, 2-chloro-N-3-pyridinyl-
CAS Number 78205-18-2
Molecular Formula C7H7ClN2O
Molecular Weight 170.5963
MDL Number MFCD00772161
SMILES ClCC(=O)Nc1cccnc1

2-Chloro-N-(pyridin-3-yl)acetamide is a highly versatile compound that finds significant utility in chemical synthesis, particularly in the field of medicinal chemistry and drug development. This compound serves as a key building block in the creation of various pharmaceutical agents and organic compounds.When used in chemical synthesis, 2-Chloro-N-(pyridin-3-yl)acetamide can undergo different reactions such as nucleophilic substitution, condensation, or cyclization to generate a diverse range of derivatives with distinct properties and functionalities. Its specific structure containing a chloro group and a pyridine moiety offers unique opportunities for selective transformations and structural modifications, making it a valuable tool for designing and synthesizing novel molecules with potential biological activities.Furthermore, the presence of the pyridine ring in 2-Chloro-N-(pyridin-3-yl)acetamide can facilitate its interaction with biological targets, making it particularly attractive for the development of bioactive compounds such as antibacterial agents, antifungals, or enzyme inhibitors. The compound's ability to modulate the biological activity of target molecules through structure-activity relationship studies enhances its significance in drug discovery and development processes.In summary, 2-Chloro-N-(pyridin-3-yl)acetamide plays a crucial role in chemical synthesis by enabling the creation of diverse molecular structures with potential pharmacological significance. Its versatility and utility in medicinal chemistry highlight its importance as a key intermediate in the synthesis of biologically active compounds.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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