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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, 2-[(2-hydroxy-1-naphthalenyl)azo]-,monosodium salt

Oc1ccc2c(c1N=Nc1ccc3c(c1S(=O)(=O)[O-])cccc3)cccc2.[Na+] Request for Quotation
Chemical Name: 1-Naphthalenesulfonic acid, 2-[(2-hydroxy-1-naphthalenyl)azo]-,monosodium salt
CAS Number: 1248-18-6
Product Number: AG007P5P(AGN-PC-0PHW85)
Synonyms:
MDL No:
Molecular Formula: C20H13N2NaO4S
Molecular Weight: 400.3830

Identification/Properties

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


Sodium 2-[(2-Hydroxynaphthyl)Azo]Naphthalenesulphonate, commonly referred to as $name$, plays a vital role in chemical synthesis as a versatile precursor and reagent. This compound is utilized as a key component in organic reactions due to its ability to undergo azo coupling reactions, yielding vibrant azo dyes. With its unique chemical structure, $name$ serves as a valuable building block in the synthesis of various organic compounds, making it an essential tool for researchers and chemists in the field. Its application in chemical synthesis extends to the creation of complex molecular structures, pharmaceutical intermediates, and specialty chemicals, showcasing its significance in the realm of organic chemistry. By leveraging the reactivity and selectivity of Sodium 2-[(2-Hydroxynaphthyl)Azo]Naphthalenesulphonate, chemists can explore a wide range of synthetic pathways, paving the way for innovative discoveries and advancements in the field of chemistry.