147281
苯磺酸钠
97%
别名:
苯磺酸 钠盐
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关于此项目
线性分子式:
C6H5SO3Na
化学文摘社编号:
分子量:
180.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39092528
UNSPSC Code:
12352100
EC Number:
208-198-2
MDL number:
Beilstein/REAXYS Number:
3918459
Assay:
97%
Form:
powder
InChI key
MZSDGDXXBZSFTG-UHFFFAOYSA-M
InChI
1S/C6H6O3S.Na/c7-10(8,9)6-4-2-1-3-5-6;/h1-5H,(H,7,8,9);/q;+1/p-1
SMILES string
[Na+].[O-]S(=O)(=O)c1ccccc1
assay
97%
form
powder
solubility
water: soluble
density
1.124 g/mL at 25 °C (lit.)
functional group
sulfonic acid
Quality Level
Application
苯磺酸钠已用于磺化聚苯乙烯树脂分子结构特征的拉曼光谱测定 。在不锈钢表面形成不同形貌的聚吡咯涂层时，它被用作电解液 。它被用于 1-丁基-3-丙腈咪唑苯磺酸酯的合成 。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Effect of sulfonate-based anions on the physicochemical properties of 1-alkyl-3-propanenitrile imidazolium ionic liquids.
Ziyada AK, et al.
New. J. Chem., 35(5), 1111-1116 (2011)
Raman spectroscopy of sulfonated polystyrene resins.
Edwards HGM, et al.
Vibrational Spectroscopy, 24(2), 213-224 (2000)
Formation of polypyrrole coatings on stainless steel in aqueous benzene sulfonate solution.
Su W and Iroh JO.
Electrochimica Acta, 42(17), 2685-2694 (1997)
Wen Huang et al.
The Journal of organic chemistry, 73(17), 6845-6848 (2008-08-07)
A novel, convenient, and efficient method has been developed for selective synthesis of spirocycle, polycycle, and di- and tetrahydronaphthalene systems from aryl-substituted propargylic alcohols by FeCl3- or TsOH-catalyzed multiple activations of unsaturated C-C bonds and C-H bonds.
Snehlata Yadav et al.
European journal of medicinal chemistry, 45(12), 5985-5997 (2010-10-26)
A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones.
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