等级
technical grade
质量水平
方案
90%
表单
solid
官能团
sulfonic acid
SMILES字符串
OS(=O)(=O)c1ccccc1
InChI
1S/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9)
InChI key
SRSXLGNVWSONIS-UHFFFAOYSA-N
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一般描述
苯磺酸(Benzenesulfonic acid)，又称为“besylic acid”，是一种有机强酸，在各种有机反应中常用作酸催化剂，包括酯化、烷基化和缩合反应。也可作为磺化剂，将磺酸(SO3H)基引入有机物用于各种染料中间体的合成。
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
M Jinish Antony et al.
The journal of physical chemistry. B, 114(3), 1314-1324 (2010-01-07)
Here, we report a unique molecular template approach, for the first time, to study the evolution of the different types of nanomaterial morphologies such as nanofiber, nanorod, nanosphere, and nanotube in a single system without changing their chemical composition or
Garry D Sisk et al.
Electrophoresis, 30(19), 3366-3371 (2009-09-04)
In this research, ion transfer across the interface between two immiscible electrolyte solutions (ITIES) was used as a method of detection in a CE separation system. This method allows for the electrochemical detection of ionic analytes that cannot be easily
Wang-Ping Ting et al.
Journal of hazardous materials, 156(1-3), 421-427 (2008-02-05)
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed. The use of UVA light and electric current as electron donors can efficiently initiate the Fenton reaction. Benzene sulfonic acid
Wenyi Huang et al.
ACS nano, 6(11), 10178-10185 (2012-10-27)
High-performance graphene nanopapers are prepared from an aqueous solution of functional graphenes with benzenesulfonic acid groups via covalent bonds. The formed hydrophobic graphene nanopapers showed the highest tensile strength of 360 MPa and Young's modulus of 102 GPa for samples
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.
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