Cas no 114394-36-4 (Sodium1-amine-2-naphthol-4-sulfonate)
Sodium1-amine-2-naphthol-4-sulfonate Chemical and Physical Properties
Names and Identifiers
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- Sodium 1-amine-2-naphthol-4-sulfonate
- 1-Amino-2-naphthol-4-sulfonic acid monosodium salt
- sodium; 4-amino-3-hydroxy-naphthalene-1-sulfonate
- 4-Amino-3-hydroxy-1-naphthalenesulfonic acid sodium salt
- Sodium 4-amino-3-hydroxynaphthalene-1-sulphonate
- sodium;4-amino-3-hydroxynaphthalene-1-sulfonate
- 1-Naphthalenesulfonic acid, 4-amino-3-hydroxy-, monosodium salt
- SODIUM 4-AMINO-3-HYDROXY-1-NAPHTHALENESULFONATE
- SCHEMBL4113728
- Sodium1-amine-2-naphthol-4-sulfonate
- TAU717J5AA
- Q27289872
- SODIUM 1-AMINO-2-HYDROXY-4-NAPHTHALENE SULFONATE
- 1-NAPHTHALENESULFONIC ACID, 4-AMINO-3-HYDROXY-, SODIUM SALT (1:1)
- DTXSID00208261
- NS00082179
- FT-0764846
- sodium 4-amino-3-hydroxy-naphthalene-1-sulfonate
- 114394-36-4
- AKOS015914482
- 1-AMINO-2-NAPHTHOL-4-SULFONIC ACID SODIUM SALT [MI]
- SODIUM 1-AMINO-2-NAPHTHOL-4-SULFONATE
- EINECS 227-728-3
- UNII-TAU717J5AA
- SODIUM 4-AMINO-3-HYDROXYNAPHTHALENE-1-SULFONATE
- 1-Amino-2-naphthol-4-sodium sulfonate
- 5959-58-0
- 1-AMINO-2-NAPHTHOL-4-SULFONIC ACID SODIUM SALT
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- Inchi: 1S/C10H9NO4S.Na/c11-10-7-4-2-1-3-6(7)9(5-8(10)12)16(13,14)15;/h1-5,12H,11H2,(H,13,14,15);/q;+1/p-1
- InChI Key: PIROYXPDJRYHBP-UHFFFAOYSA-M
- SMILES: S(C1C=C(C(=C2C=CC=CC2=1)N)O)(=O)(=O)[O-].[Na+]
Computed Properties
- Exact Mass: 261.00700
- Monoisotopic Mass: 261.00717319g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 17
- Rotatable Bond Count: 1
- Complexity: 356
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 112?2
Experimental Properties
- PSA: 111.83000
- LogP: 2.69370
Sodium1-amine-2-naphthol-4-sulfonate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | S224600-50mg |
Sodium1-amine-2-naphthol-4-sulfonate |
114394-36-4 | 50mg |
$ 220.00 | 2022-06-03 | ||
| TRC | S224600-100mg |
Sodium1-amine-2-naphthol-4-sulfonate |
114394-36-4 | 100mg |
$ 365.00 | 2022-06-03 | ||
| TRC | S224600-250mg |
Sodium1-amine-2-naphthol-4-sulfonate |
114394-36-4 | 250mg |
$ 725.00 | 2022-06-03 |
Sodium1-amine-2-naphthol-4-sulfonate Related Literature
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Kanhu Charan Rout,Biplab Mondal Dalton Trans. 2015 44 1829
Additional information on Sodium1-amine-2-naphthol-4-sulfonate
Sodium 1-Amine-2-Naphthol-4-Sulfonate: A Comprehensive Overview
Sodium 1-Amine-2-Naphthol-4-Sulfonate, with the CAS number 114394-36-4, is a versatile compound that has garnered significant attention in various scientific and industrial applications. This compound, often referred to as Sodium 1-Amine-2-Naphthol-4-Sulfonate, is a derivative of naphthol, a polycyclic aromatic hydrocarbon with two fused benzene rings. The sulfonate group attached to the naphthol structure imparts unique chemical properties, making it suitable for a wide range of uses.
The structure of Sodium 1-Amine-2-Naphthol-4-Sulfonate is characterized by an amine group (-NH2) at position 1 and a sulfonate group (-SO3Na) at position 4 of the naphthol ring system. This configuration not only enhances its solubility in polar solvents but also contributes to its reactivity in various chemical reactions. Recent studies have highlighted its potential as a building block in organic synthesis, particularly in the development of advanced materials and pharmaceutical intermediates.
One of the most notable applications of Sodium 1-Amine-2-Naphthol-4-Sulfonate is in the field of pharmaceutical chemistry. Researchers have explored its role as an intermediate in the synthesis of bioactive compounds, including anti-inflammatory and antiviral agents. For instance, a study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent inhibitory activity against certain viral enzymes, paving the way for potential antiviral drug development.
In addition to its pharmaceutical applications, Sodium 1-Amine-2-Naphthol-4-Sulfonate has found utility in the textile industry. Its ability to act as a reducing agent in dyeing processes has made it a valuable component in the production of high-quality textiles. Recent advancements in sustainable textile manufacturing have further underscored its importance, as researchers seek eco-friendly alternatives to traditional dyeing agents.
The synthesis of Sodium 1-Amine-2-Naphthol-4-Sulfonate involves a multi-step process that typically begins with the sulfonation of naphthalene derivatives. Modern synthetic methods have focused on optimizing reaction conditions to improve yield and purity. For example, a study reported in Green Chemistry highlighted the use of microwave-assisted synthesis to accelerate the reaction process while minimizing environmental impact.
From an analytical standpoint, Sodium 1-Amine-2-Naphthol-4-Sulfonate has been extensively studied using advanced spectroscopic techniques such as UV-vis spectroscopy and NMR spectroscopy. These studies have provided valuable insights into its electronic structure and molecular interactions, which are critical for understanding its reactivity and stability under various conditions.
Looking ahead, ongoing research into Sodium 1-Amine-2-Naphthol-4-Sulfonate is expected to uncover new applications across diverse fields. Its unique combination of structural features makes it a promising candidate for use in nanotechnology, where it could serve as a precursor for functional materials with tailored properties.
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