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  2. 2,7-Naphthalenedisulfonic acid,4,5-dihydroxy-3,6-bis[(4-methyl-2-sulfophenyl)azo]-

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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)-

2,7-Naphthalenedisulfonic acid,4,5-dihydroxy-3,6-bis[(4-methyl-2-sulfophenyl)azo]-

Cc1ccc(c(c1)S(=O)(=O)O)N=Nc1c(O)c2c(cc1S(=O)(=O)O)cc(c(c2O)N=Nc1ccc(cc1S(=O)(=O)O)C)S(=O)(=O)O Request for Quotation
Chemical Name: 2,7-Naphthalenedisulfonic acid,4,5-dihydroxy-3,6-bis[(4-methyl-2-sulfophenyl)azo]-
CAS Number: 14979-11-4
Product Number: AG001M0S(AGN-PC-0Q3TSI)
Synonyms:
MDL No:
Molecular Formula: C24H20N4O14S4
Molecular Weight: 716.6940

Identification/Properties

Properties
MP:
>300°C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
716.7g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
18
Rotatable Bond Count:
8
Exact Mass:
715.985886g/mol
Monoisotopic Mass:
715.985886g/mol
Topological Polar Surface Area:
341Ų
Heavy Atom Count:
46
Formal Charge:
0
Complexity:
1480
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:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dihydroxy-3,6-bis((4-methyl-2-sulfophenyl)diazenyl)naphthalene-2,7-disulfonic acid is a versatile compound widely used in chemical synthesis. As a diazo dye, it is commonly employed as a colorimetric indicator in various analytical chemistry applications. In addition, this compound plays a crucial role in organic synthesis as a reagent for diazotization reactions, which are key transformations in the preparation of azo dyes and a variety of other organic compounds. Its unique chemical structure and properties make it a valuable tool for creating new molecules with specific functionalities, making it indispensable in the field of synthetic chemistry.