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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-[(2-amino-4-pyrimidinyl)amino]-, hydrochloride (1:1)

Nc1nccc(n1)Nc1ccc(cc1)S(=O)(=O)N.Cl Request for Quotation
Chemical Name: Benzenesulfonamide,4-[(2-amino-4-pyrimidinyl)amino]-, hydrochloride (1:1)
CAS Number: 22199-93-5
Product Number: AG019P5L(AGN-PC-0QYU0N)
Synonyms:
MDL No:
Molecular Formula: C10H12ClN5O2S
Molecular Weight: 301.7526

Identification/Properties

Computed Properties
Molecular Weight:
301.749g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
301.04g/mol
Monoisotopic Mass:
301.04g/mol
Topological Polar Surface Area:
132A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
361
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-[(2-Aminopyrimidin-4-yl)amino]benzene-1-sulfonamide Hydrochloride is a versatile compound widely utilized in chemical synthesis processes. In organic chemistry, this compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and materials. Its unique molecular structure allows for the efficient formation of complex molecules through reactions such as coupling, substitution, and condensation. Additionally, the presence of the sulfonamide group imparts desirable properties for medicinal chemistry applications, enhancing biological activities and target interactions. Overall, the strategic incorporation of 4-[(2-Aminopyrimidin-4-yl)amino]benzene-1-sulfonamide Hydrochloride in chemical synthesis enables the synthesis of diverse compounds with valuable industrial and research implications.