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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)-

Sulfalene

COc1nccnc1NS(=O)(=O)c1ccc(cc1)N Request for Quotation
Chemical Name: Sulfalene
CAS Number: 152-47-6
Product Number: AG003KRK(AGN-PC-0WAJPB)
Synonyms:
MDL No:
Molecular Formula: C11H12N4O3S
Molecular Weight: 280.3030

Identification/Properties

Properties
MP:
174-178 °C
BP:
488.6 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.6200 (estimate)
Computed Properties
Molecular Weight:
280.302g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
280.063g/mol
Monoisotopic Mass:
280.063g/mol
Topological Polar Surface Area:
116A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
376
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-N-(3-methoxypyrazin-2-yl)benzenesulfonamide is a versatile compound widely employed in chemical synthesis for its important role as a building block in organic chemistry. This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity. Its incorporation into molecular structures allows for the introduction of specific functionalities and properties, making it a valuable component in the design and development of novel compounds with desired biological activities. In addition, the presence of the sulfonamide group confers enhanced water solubility and bioavailability to the final products, further expanding the potential applications of this compound in the field of medicinal chemistry. Its systematic approach to chemical synthesis offers opportunities for the creation of diverse chemical entities with tailored properties for a range of industrial and research purposes.