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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)-

5-Quinolinesulfonicacid, 8-hydroxy-7-[2-(6-sulfo-2-naphthalenyl)diazenyl]-

O=C1C(=NNc2ccc3c(c2)ccc(c3)S(=O)(=O)O)C=C(c2c1nccc2)S(=O)(=O)O Request for Quotation
Chemical Name: 5-Quinolinesulfonicacid, 8-hydroxy-7-[2-(6-sulfo-2-naphthalenyl)diazenyl]-
CAS Number: 56990-57-9
Product Number: AG00EEGK(AGN-PC-0OCHHH)
Synonyms:
MDL No: MFCD09971104
Molecular Formula: C19H13N3O7S2
Molecular Weight: 459.4524

Identification/Properties

Computed Properties
Molecular Weight:
459.447g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
4
Exact Mass:
459.019g/mol
Monoisotopic Mass:
459.019g/mol
Topological Polar Surface Area:
183A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
883
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

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Chemical Structure


5-Quinolinesulfonicacid, 8-hydroxy-7-[2-(6-sulfo-2-naphthalenyl)diazenyl]- is a versatile compound widely employed in chemical synthesis as a powerful dye precursor. With its unique molecular structure, this compound plays a crucial role in the creation of vibrant dyes used in various industries including textiles, cosmetics, and printing. Its reactive functional groups make it ideal for coupling reactions with different substrates, allowing for the synthesis of custom dyes tailored to specific applications. Additionally, the presence of the hydroxy and sulfonic acid groups provides solubility characteristics that enhance the compound's compatibility with different reaction conditions, further expanding its utility in chemical synthesis processes.