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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)-

sodium;4-[[4-(diethylamino)phenyl]diazenyl]benzenesulfonate

CCN(c1ccc(cc1)N=Nc1ccc(cc1)S(=O)(=O)[O-])CC.[Na+] Request for Quotation
Chemical Name: sodium;4-[[4-(diethylamino)phenyl]diazenyl]benzenesulfonate
CAS Number: 62758-12-7
Product Number: AG00E9IH(AGN-PC-047737)
Synonyms:
MDL No:
Molecular Formula: C16H18N3NaO3S
Molecular Weight: 355.3872

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Computed Properties
Molecular Weight:
355.388g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
355.097g/mol
Monoisotopic Mass:
355.097g/mol
Topological Polar Surface Area:
93.5A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
475
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzenesulfonic acid, 4-[2-[4-(diethylamino)phenyl]diazenyl]-, sodium salt (1:1) is a versatile compound commonly used in chemical synthesis due to its unique properties. One significant application of this compound is in the realm of organic chemistry, where it serves as a key reagent in various reactions. Particularly, it is utilized in the synthesis of azo dyes, which are important compounds widely employed in industries such as textiles, printing, and cosmetics. The presence of the diazenyl group in the molecule enables it to participate in azo coupling reactions with aromatic amines, resulting in the formation of vibrant and stable azo dyes. This compound's role in chemical synthesis extends beyond dye formation, as it can also be utilized in the production of pharmaceuticals, agrochemicals, and materials science applications. Its versatility and reactivity make it a valuable tool for advancing synthetic organic chemistry methodologies and creating novel compounds with diverse functionalities.