2,4-dichloro-N-propan-2-yl-N-[2-(propan-2-ylamino)ethyl]benzenesulfonamide


Chemical Name: 2,4-dichloro-N-propan-2-yl-N-[2-(propan-2-ylamino)ethyl]benzenesulfonamide
CAS Number: 946387-07-1
Product Number: AG01ENOZ(AGN-PC-0KX5VQ)
Synonyms:
MDL No: MFCD00129453
Molecular Formula: C14H22Cl2N2O2S
Molecular Weight: 353.3077

Identification/Properties


Computed Properties
Molecular Weight:
353.302g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
352.078g/mol
Monoisotopic Mass:
352.078g/mol
Topological Polar Surface Area:
57.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
410
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

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 2,4-Dichloro-N-(1-methylethyl)-N-[2-[(1-methylethyl)amino]ethyl]benzenesulfonamide, is commonly used in chemical synthesis as a versatile building block for the creation of complex organic molecules. Its unique structure makes it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, this compound can serve as a key precursor for the introduction of functional groups such as amines, sulfonamides, and alkyl groups. By utilizing the reactive chloro groups on the benzene ring, chemists can selectively modify the molecule to tailor its properties for specific applications. Additionally, the presence of the isopropyl and ethyl groups provides opportunities for stereochemical control and further diversification of the final product.Overall, the application of 2,4-Dichloro-N-(1-methylethyl)-N-[2-[(1-methylethyl)amino]ethyl]benzenesulfonamide in chemical synthesis allows for the efficient construction of complex molecules with precise control over structure and functionality.