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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)-

1-Naphthalenesulfonic acid, 8-(phenylamino)-, magnesium salt (2:1)

[O-]S(=O)(=O)c1cccc2c1c(ccc2)Nc1ccccc1.[O-]S(=O)(=O)c1cccc2c1c(ccc2)Nc1ccccc1.[Mg+2] Request for Quotation
Chemical Name: 1-Naphthalenesulfonic acid, 8-(phenylamino)-, magnesium salt (2:1)
CAS Number: 18108-68-4
Product Number: AG0022OH(AGN-PC-0QBYWW)
Synonyms:
MDL No:
Molecular Formula: C32H24MgN2O6S2
Molecular Weight: 620.9778

Identification/Properties

Properties
MP:
>202°C (dec.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Solubility:
H2O: soluble50mg/mL
Computed Properties
Molecular Weight:
620.977g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
4
Exact Mass:
620.093g/mol
Monoisotopic Mass:
620.093g/mol
Topological Polar Surface Area:
155A^2
Heavy Atom Count:
43
Formal Charge:
0
Complexity:
426
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Magnesium 8-(phenylamino)naphthalene-1-sulfonate, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a catalyst in various organic reactions, particularly in the field of synthetic chemistry. Its unique structure and properties make it an essential component in the formation of complex organic molecules.One of the key applications of Magnesium 8-(phenylamino)naphthalene-1-sulfonate is in the realm of metal-catalyzed reactions. This compound serves as an effective catalyst in cross-coupling reactions, allowing for the formation of carbon-carbon and carbon-heteroatom bonds with high efficiency. Its use in Suzuki-Miyaura couplings, Heck reactions, and other important transformations showcases its significance in modern synthetic methodologies.Furthermore, Magnesium 8-(phenylamino)naphthalene-1-sulfonate plays a crucial role in the activation of substrates and facilitating key bond-forming steps in complex organic syntheses. Its ability to promote challenging transformations under mild reaction conditions makes it a valuable tool for chemists working in the development of pharmaceuticals, agrochemicals, and other fine chemicals.Overall, Magnesium 8-(phenylamino)naphthalene-1-sulfonate stands as a pivotal reagent in chemical synthesis, enabling chemists to access novel compounds and streamline the process of molecule construction. Its versatility and efficacy make it a staple in the toolkit of synthetic chemists striving to push the boundaries of organic chemistry.