推荐产品
等级
AR
蒸汽密度
5.9 (vs air)
产品线
Vetec™
方案
≥99%
mp
103-106 °C (lit.)
官能团
tosylate
SMILES字符串
[H]O[H].Cc1ccc(cc1)S(O)(=O)=O
InChI
1S/C7H8O3S.H2O/c1-6-2-4-7(5-3-6)11(8,9)10;/h2-5H,1H3,(H,8,9,10);1H2
InChI key
KJIFKLIQANRMOU-UHFFFAOYSA-N
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法律信息
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Zhiqiang Ji et al.
Inorganic chemistry, 49(4), 1337-1346 (2010-01-23)
Two back-to-back terpyridine ligands using fluorenyl as bridging group (1-L and 2-L) and their corresponding dinuclear platinum(II) complexes (1 and 2) were synthesized and characterized. Their electronic absorption, photoluminescence, and the triplet transient difference absorption were systematically investigated. Both ligands
Jhonny Azuaje et al.
ACS combinatorial science, 13(1), 89-95 (2011-01-21)
We document here the use of polymer-supported p-toluenesulfonic acid as a highly effective, robust, economical and eco-friendly isocyanide scavenger. The herein described strategy circumvent the intense and repulsive odor of volatile isocyanides, enabling simplified and odorless workup and purifications. The
Aditya Kulkarni et al.
Organic letters, 13(19), 5124-5127 (2011-09-10)
An environmentally benign procedure for the hydrogenation of unprotected indoles is described. The hydrogenation reaction is catalyzed by Pt/C and activated by p-toluenesulfonic acid in water as a solvent. The efficacy of the method is illustrated by the hydrogenation of
Daniel C Yee et al.
The FEBS journal, 280(22), 5780-5800 (2013-08-29)
Visual rhodopsins are recognized members of the large and diverse family of G protein-coupled receptors (GPCRs), but their evolutionary origin and relationships to other proteins are not known. In a previous paper [Shlykov MA, Zheng WH, Chen JS & Saier
Koneni V Sashidhara et al.
Bioorganic & medicinal chemistry letters, 22(12), 3926-3930 (2012-05-23)
First synthesis of novel coumarin-trioxane hybrids is reported. The synthesis was achieved via condensation of β-hydroxyhydroperoxides with coumarinic-aldehydes in presence of p-toluenesulfonic acid in good yields and the novel hybrids were evaluated for their antimalarial activity both in vitro and
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