Cas no 16704-71-5 (3-(diphenylphosphanyl)benzene-1-sulfonic acid)
3-(diphenylphosphanyl)benzene-1-sulfonic acid Chemical and Physical Properties
Names and Identifiers
-
- Benzenesulfonicacid, 3-(diphenylphosphino)-
- 3-diphenylphosphanylbenzenesulfonic acid
- (m-sulfophenyl)-diphenyl phosphine
- 3-(diphenylphosphanyl)benzene-1-sulfonic acid
- 3-(diphenylphosphanyl)benzenesulfonic acid
- 3-(diphenylphosphine)-benzenesulfonic acid
- 3-(diphenylphosphino)benzenesulfonic acid
- 3-diphenylphosphino-benzenesulfonic acid
- AC1L50QS
- AG-J-92017
- CTK0G9381
- meta-monosulfonated triphenylphosphine
- m-sulfophenyldiphenylphosphine
- SCHEMBL1313640
- 16704-71-5
- CS-0203242
- AKOS000814245
- EN300-119475
- DTXSID00276743
- 3-(diphenylphosphino)benzenesulfonicacid
- Benzenesulfonic acid, 3-(diphenylphosphino)-
-
- Inchi: 1S/C18H15O3PS/c19-23(20,21)18-13-7-12-17(14-18)22(15-8-3-1-4-9-15)16-10-5-2-6-11-16/h1-14H,(H,19,20,21)
- InChI Key: ITPOKAFWZBFZCV-UHFFFAOYSA-N
- SMILES: S(C1=CC=CC(=C1)P(C1C=CC=CC=1)C1C=CC=CC=1)(=O)(=O)O
Computed Properties
- Exact Mass: 342.04805
- Monoisotopic Mass: 342.048
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 23
- Rotatable Bond Count: 4
- Complexity: 443
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.4
- Topological Polar Surface Area: 62.8?2
Experimental Properties
- PSA: 54.37
- LogP: 3.77230
3-(diphenylphosphanyl)benzene-1-sulfonic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-119475-0.05g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 0.05g |
$30.0 | 2023-02-18 | |
| Enamine | EN300-119475-0.1g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 0.1g |
$45.0 | 2023-02-18 | |
| Enamine | EN300-119475-0.25g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 0.25g |
$64.0 | 2023-02-18 | |
| Enamine | EN300-119475-0.5g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 0.5g |
$101.0 | 2023-02-18 | |
| Enamine | EN300-119475-1.0g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 1g |
$0.0 | 2023-06-08 | |
| Enamine | EN300-119475-2.5g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 2.5g |
$214.0 | 2023-02-18 | |
| Enamine | EN300-119475-5.0g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 5.0g |
$356.0 | 2023-02-18 | |
| Enamine | EN300-119475-10.0g |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92% | 10.0g |
$639.0 | 2023-02-18 | |
| Enamine | EN300-119475-50mg |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92.0% | 50mg |
$30.0 | 2023-10-03 | |
| Enamine | EN300-119475-100mg |
3-(diphenylphosphanyl)benzene-1-sulfonic acid |
16704-71-5 | 92.0% | 100mg |
$45.0 | 2023-10-03 |
3-(diphenylphosphanyl)benzene-1-sulfonic acid Related Literature
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Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
Additional information on 3-(diphenylphosphanyl)benzene-1-sulfonic acid
Comprehensive Overview of 3-(Diphenylphosphanyl)benzene-1-sulfonic Acid (CAS No. 16704-71-5)
3-(Diphenylphosphanyl)benzene-1-sulfonic acid (CAS No. 16704-71-5) is a highly versatile organophosphorus compound widely utilized in catalysis, material science, and pharmaceutical research. Its unique structure, featuring a diphenylphosphine group and a sulfonic acid moiety, enables it to act as a bifunctional ligand or catalyst in cross-coupling reactions, hydrogenation, and other synthetic transformations. The compound's water-soluble properties, attributed to the sulfonic acid group, make it particularly valuable in green chemistry applications, aligning with the growing demand for sustainable chemical processes.
In recent years, the demand for efficient catalysts and ligands has surged, driven by advancements in pharmaceutical intermediates and fine chemical synthesis. Researchers frequently search for terms like "phosphine-based catalysts" or "sulfonated ligands," reflecting the compound's relevance in modern chemistry. 3-(Diphenylphosphanyl)benzene-1-sulfonic acid stands out due to its ability to facilitate reactions under mild conditions, reducing energy consumption and waste generation—a critical consideration in green chemistry and ESG (Environmental, Social, and Governance)-focused industries.
The compound's applications extend to asymmetric synthesis, where its chiral derivatives are employed to produce enantiomerically pure compounds. This is particularly significant in the development of active pharmaceutical ingredients (APIs), as regulatory agencies increasingly emphasize chiral purity in drug formulations. Searches for "chiral phosphine ligands" or "sulfonic acid catalysts" often lead to discussions about this compound, highlighting its role in cutting-edge research.
From a material science perspective, 3-(Diphenylphosphanyl)benzene-1-sulfonic acid is explored for its potential in polymer modification and surface functionalization. Its sulfonic acid group can enhance the hydrophilicity of polymers, making it useful in ion-exchange membranes for fuel cells or water purification systems. This aligns with the global push toward renewable energy and clean water technologies, topics frequently searched in academic and industrial circles.
In summary, 3-(Diphenylphosphanyl)benzene-1-sulfonic acid (CAS No. 16704-71-5) is a multifaceted compound with broad applications in catalysis, pharmaceuticals, and materials science. Its combination of phosphine and sulfonic acid functionalities makes it a valuable tool for researchers aiming to develop sustainable and high-efficiency chemical processes. As industries prioritize green chemistry and chiral synthesis, this compound is poised to remain a focal point of innovation.
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