1. Home
  2. Benzenesulfonamide, 4-amino-N-(1,1-dimethylethyl)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenesulfonamide, 4-amino-N-(1,1-dimethylethyl)-

CC(NS(=O)(=O)c1ccc(cc1)N)(C)C Request for Quotation
Chemical Name: Benzenesulfonamide, 4-amino-N-(1,1-dimethylethyl)-
CAS Number: 209917-48-6
Product Number: AG0035F1(AGN-PC-0JWPZA)
Synonyms:
MDL No:
Molecular Formula: C10H16N2O2S
Molecular Weight: 228.3112

Identification/Properties

Properties
MP:
128-130°C
BP:
374.8 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
228.31g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
228.093g/mol
Monoisotopic Mass:
228.093g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
292
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Amino-N-(tert-butyl)benzenesulfonamide, also known simply as $name$, is a versatile compound commonly used in organic chemical synthesis. This chemical plays a crucial role as a building block in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it an essential intermediate in the production of a wide range of organic compounds.One of the key applications of 4-Amino-N-(tert-butyl)benzenesulfonamide in chemical synthesis is its use as a nucleophilic coupling partner in the formation of carbon-carbon and carbon-nitrogen bonds. This compound can participate in a variety of reactions, including Suzuki-Miyaura cross-coupling, Buchwald-Hartwig amination, and Ullmann-type coupling reactions. These reactions enable the introduction of the $name$ moiety into complex organic molecules, allowing for the synthesis of diverse chemical libraries with potential biological activities.Moreover, 4-Amino-N-(tert-butyl)benzenesulfonamide serves as a valuable precursor for the preparation of sulfonamide derivatives, which are widely utilized in medicinal chemistry. Through functional group transformations and further derivatization, this compound can be tailored to impart specific physicochemical properties or enhance biological activity in target molecules. Its sulfonamide functionality also provides opportunities for hydrogen bonding interactions and can serve as a pharmacophore in drug design.In summary, 4-Amino-N-(tert-butyl)benzenesulfonamide is a versatile and essential reagent in chemical synthesis, offering a wide range of applications in the development of pharmaceuticals and other bioactive molecules. Its synthetic utility and structural features make it a valuable tool for organic chemists seeking to access novel compounds and explore new chemical space for potential therapeutic agents.