Cas no 6791-71-5 (Sulphathiazole sodium pentahydrate)
6791-71-5 structure
Product Name:Sulphathiazole sodium pentahydrate
CAS No:6791-71-5
MF:C9H18N3NaO7S2
MW:367.374890804291
CID:967766
Update Time:2023-08-02
Sulphathiazole sodium pentahydrate Chemical and Physical Properties
Names and Identifiers
-
- sodium sulfathiazole
- Sulphathiazole sodium pentahydrate
- ST7PF0D71H
- Sulfathiazole sodium pentahydrate
- Sodium sulfathiazole pentahydrate
- Sulphathiazole sodium pentahydrate [WHO-DD]
- Sulfathiazole sodium 5h2o
- C9H8N3NaO2S2.5H2O
- Sulfanilamide, N1-2-thiazolyl-, monosodium salt, pentahydrate
- 8167AF
- Benzenesulfonamide, 4-amino-N-2-thiazolyl-, sodium salt, hydrate (1:1:5)
- Benzenesulfonamide, 4-amino-N-2-thiazolyl-, monosodium salt, pentahydrate
- Q27289386
-
- Inchi： 1S/C9H8N3O2S2.Na.5H2O/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9;;;;;;/h1-6H,10H2;;5*1H2/q-1;+1;;;;;
- InChI Key： NKCXOSYACXARER-UHFFFAOYSA-N
- SMILES： S(C1C=CC(=CC=1)N)([N-]C1=NC=CS1)(=O)=O.[Na+].O.O.O.O.O
Computed Properties
- Exact Mass: 367.048
- Monoisotopic Mass: 367.048
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 6
- Hydrogen Bond Acceptor Count: 11
- Heavy Atom Count: 22
- Rotatable Bond Count: 3
- Complexity: 326
- Covalently-Bonded Unit Count: 7
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 116
Sulphathiazole sodium pentahydrate Related Literature
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Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
-
Marta Liras,Isabel Quijada-Garrido,Marta Palacios-Cuesta,Sonia Mu?oz-Durieux,Olga García Polym. Chem., 2014,5, 433-442
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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4. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
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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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