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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)-

2-aminopyrimidine-5-sulfonamide

Nc1ncc(cn1)S(=O)(=O)N Request for Quotation
Chemical Name: 2-aminopyrimidine-5-sulfonamide
CAS Number: 99171-23-0
Product Number: AG00IK8F(AGN-PC-09S0U3)
Synonyms:
MDL No:
Molecular Formula: C4H6N4O2S
Molecular Weight: 174.1810

Identification/Properties

Computed Properties
Molecular Weight:
174.178g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
174.021g/mol
Monoisotopic Mass:
174.021g/mol
Topological Polar Surface Area:
120A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
213
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Aminopyrimidine-5-sulfonamide, a versatile compound in chemical synthesis, is widely utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. This compound offers a valuable synthetic route for the construction of heterocyclic structures due to its unique reactivity and functional group compatibility. In the pharmaceutical industry, 2-Aminopyrimidine-5-sulfonamide serves as a vital intermediate in the synthesis of novel antibacterial, antifungal, and antiviral agents. Additionally, its ability to undergo diverse chemical transformations makes it a valuable tool in the development of new therapeutic compounds. In agrochemical synthesis, this compound plays a crucial role in the production of pesticides and herbicides with improved efficacy and environmental safety. Furthermore, the incorporation of 2-Aminopyrimidine-5-sulfonamide in the synthesis of fine chemicals enables the creation of specialty products with enhanced properties and functionality. Its broad application in chemical synthesis highlights its significance as a key component in the development of various valuable compounds across different industries.