Interesting facts
Interesting Facts about Disodium 4-[2-[4,6-Dioxo-5-[(4-Sulfonato-1-naphthyl)hydrazono]cyclohex-2-en-1-ylidene]hydrazino]naphthalene-1-sulfonate
This intriguing compound, commonly referred to as a sulfonated derivative of naphthalene, showcases the fascinating intersection of organic chemistry and material science. Here are some insightful aspects to consider:
- Complex Structure: Disodium 4-[2-[4,6-Dioxo-5-[(4-Sulfonato-1-naphthyl)hydrazono]cyclohex-2-en-1-ylidene]hydrazino]naphthalene-1-sulfonate is characterized by a complex molecular architecture, featuring multiple functional groups, including hydrazone links and sulfonate moieties.
- Applications in Dyes: This compound is notable for its applications in dye chemistry, where it can act as a dyeing agent due to its extensive conjugated system, allowing for vibrant coloration in a variety of materials.
- Biological Relevance: The incorporation of sulfonate groups enhances water solubility, making this compound suitable for various biological applications, including in the development of pharmaceuticals and biologically active compounds.
- Synthesis and Reactivity: Understanding the synthetic pathways and reactivity of this compound provides insight into complex chemical reactions that involve multi-step processes, showcasing the creativity required in organic synthesis.
- Eco-Friendly Innovations: Researchers are actively exploring derivatives of such compounds as eco-friendly alternatives in industrial applications, thereby minimizing environmental impact without sacrificing performance.
As you delve deeper into the study of disodium 4-[2-[4,6-Dioxo-5-[(4-Sulfonato-1-naphthyl)hydrazono]cyclohex-2-en-1-ylidene]hydrazino]naphthalene-1-sulfonate, one might reflect on the words of the renowned chemist Robert H. Grubbs, who once said, “The beauty of science is that it offers a solution to the problems we face, often in unexpected ways.” This compound exemplifies such ingenuity and versatility.
Synonyms
DTXSID2041707
C.I. ACID BROWN 14, DISODIUM SALT
1-Naphthalenesulfonic acid, 4,4'-((2,4-dihydroxy-1,3-phenylene)bis(2,1-diazenediyl))bis-, sodium salt (1:2)
1-Naphthalenesulfonic acid, 4,4'-[(2,4-dihydroxy-1,3-phenylene)bis(2,1-diazenediyl)]bis-, sodium salt (1:2)
DTXCID001474357
C.I. Acid Brown 14, disodium salt (8CI)
5850-16-8
Acid Brown 14
Acid Brown M
C.I. 20195
Disodium 4,4'-(2,4-dihydroxy-1,3-phenylene)bis(azo)bisnaphthalene-1-sulphonate
UTIACSXEVKXHPT-UHFFFAOYSA-L
Sodium 4,4'-((2,4-dihydroxy-1,3-phenylene)bis(diazene-2,1-diyl))bis(naphthalene-1-sulfonate)
C.I.Acid Brown 14 (C.I.20195)
Q27272603
disodium 4-(2-{4,6-dioxo-5-[2-(4-sulfonatonaphthalen-1-yl)hydrazin-1-ylidene]cyclohex-2-en-1-ylidene}hydrazin-1-yl)naphthalene-1-sulfonate
disodium;4-[2-[4,6-dioxo-5-[(4-sulfonatonaphthalen-1-yl)hydrazinylidene]cyclohex-2-en-1-ylidene]hydrazinyl]naphthalene-1-sulfonate
Solubility of Disodium 4-[2-[4,6-Dioxo-5-[(4-Sulfonato-1-Naphthyl)Hydrazono]Cyclohex-2-En-1-Ylidene]Hydrazino]Naphthalene-1-Sulfonate
Disodium 4-[2-[4,6-dioxo-5-[(4-sulfonato-1-naphthyl)hydrazono]cyclohex-2-en-1-ylidene]hydrazino]naphthalene-1-sulfonate exhibits considerable solubility in aqueous solutions due to the presence of sulfonate groups that enhance its ionic character. The solubility characteristics can be summarized as follows:
This compound's solubility is significant for its utility in applications such as dye chemistry, where it functions effectively in aqueous systems. As quoted from solubility studies, "the presence of sulfonate groups is crucial in enhancing solubility in polar solvents."
Hence, the capacity to dissolve efficiently makes it a valuable compound for researchers and industrial applications alike.