N-(4-chlorophenyl)-2,6-difluorobenzamide


Chemical Name: N-(4-chlorophenyl)-2,6-difluorobenzamide
CAS Number: 122987-01-3
Product Number: AG000JV0(AGN-PC-0KGFAE)
Synonyms:
MDL No:
Molecular Formula: C13H8ClF2NO
Molecular Weight: 267.6585

Identification/Properties


Properties
MP:
147 - 148°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
267.66g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
267.026g/mol
Monoisotopic Mass:
267.026g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
285
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



N-(4-Chlorophenyl)-2,6-difluorobenzamide, commonly referred to as $name$, is a versatile chemical compound that finds wide application in chemical synthesis processes. Its unique molecular structure and properties make it an excellent reagent for various synthetic reactions in the field of organic chemistry.$name$ is frequently used as a key building block in the synthesis of pharmaceutical compounds, agrochemicals, and other specialty chemicals. Its presence as a reagent in a reaction mixture can facilitate the formation of complex molecular structures with high efficiency and selectivity. In particular, the 4-chlorophenyl and 2,6-difluorobenzamide moieties in $name$ play crucial roles in directing the regioselectivity and stereoselectivity of numerous chemical transformations.Moreover, $name$ is valued for its compatibility with a wide range of chemical reactions, including cross-coupling reactions, nucleophilic substitutions, and amide bond formations. The incorporation of $name$ into synthetic sequences enables chemists to access novel compounds, intermediates, and derivatives that have important applications in the fields of medicine, agriculture, and materials science.In summary, the strategic incorporation of N-(4-Chlorophenyl)-2,6-difluorobenzamide ($name$) in chemical synthesis offers a powerful tool for the construction of diverse molecular architectures with tailored properties and functionalities. Its versatility and efficacy make it an indispensable reagent for advancing the frontiers of synthetic organic chemistry.