2,4-dichlorobenzenecarboximidamide;hydrochloride


Chemical Name: 2,4-dichlorobenzenecarboximidamide;hydrochloride
CAS Number: 154505-50-7
Product Number: AG007XHR(AGN-PC-079GVF)
Synonyms:
MDL No:
Molecular Formula: C7H7Cl3N2
Molecular Weight: 225.5029

Identification/Properties


Computed Properties
Molecular Weight:
225.497g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
223.967g/mol
Monoisotopic Mass:
223.967g/mol
Topological Polar Surface Area:
49.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
161
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:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,4-Dichlorobenzimidamide hydrochloride is a vital compound widely used in chemical synthesis due to its unique properties and versatile applications. As a key reagent in organic chemistry, this compound plays a crucial role in various synthetic processes. Its ability to act as an efficient catalyst in a range of reactions makes it an indispensable tool for chemists working in diverse fields such as pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 2,4-Dichlorobenzimidamide hydrochloride is commonly employed as a catalyst for the formation of complex organic molecules. Its high reactivity and selectivity facilitate the selective bond formation and functional group transformations required for the synthesis of intricate chemical structures. This compound is particularly valuable in the construction of heterocyclic compounds, which are essential building blocks in pharmaceutical research and the development of new materials.Moreover, 2,4-Dichlorobenzimidamide hydrochloride's versatile nature enables its use in a range of transformations such as cross-coupling reactions, oxidative coupling, and asymmetric catalysis. Its ability to promote various reaction pathways and control stereochemistry makes it a valuable tool for chemists seeking to streamline synthetic processes and improve overall efficiency.Overall, 2,4-Dichlorobenzimidamide hydrochloride serves as a cornerstone in modern chemical synthesis, enabling scientists to access new chemical entities and enhance the efficiency of synthetic routes. Its broad applicability and exceptional reactivity make it an indispensable component in the toolkit of synthetic chemists striving to push the boundaries of chemical knowledge and innovation.