推荐产品
等级
produced by Wacker Chemie AG, Burghausen, Germany
方案
≥98.0% (T)
表单
liquid
折射率
n20/D 1.36 (lit.)
沸点
77 °C/80 mmHg (lit.)
密度
1.228 g/mL at 25 °C (lit.)
SMILES字符串
C[Si](C)(C)OS(=O)(=O)C(F)(F)F
InChI
1S/C4H9F3O3SSi/c1-12(2,3)10-11(8,9)4(5,6)7/h1-3H3
InChI key
FTVLMFQEYACZNP-UHFFFAOYSA-N
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其他说明
根据要求提供批量采购价
警示用语：
Danger
危险声明
危险分类
Flam. Liq. 3 - Skin Corr. 1B
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
77.0 °F - closed cup
闪点(°C)
25 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Feng Liu et al.
The Journal of organic chemistry, 74(15), 5699-5702 (2009-06-10)
By treatment with TMSOTf/Et3N, N-(2-cyanoarylmethyl)-substituted acrylamides or beta-ketoamides underwent N-addition cascades under mild conditions to afford the corresponding pyrrolo[1,2-a]pyrimidin-4(6H)-ones as the formal [4 + 2] cycloaddition products in high yields.
Sajal Kumar Maity et al.
Carbohydrate research, 354, 40-48 (2012-05-01)
N-(p-Methylphenylthio)-ε-caprolactam (1) in combination with trimethylsilyl trifluoromethanesulfonate (TMSOTf) provides an efficient thiophilic promoter system, capable of activating different thioglycosides. Both 'armed' and 'disarmed' thioglycosyl donors were activated for glycosidic bond formation. Notably, this reagent combination works well in reactivity-based one-pot
Cheng-Chung Wang et al.
Nature protocols, 3(1), 97-113 (2008-01-15)
Detailed protocols for the regioselective protection of individual hydroxyls in monosaccharide units are described here. This expedient methodology incorporates up to seven reaction sequences, obviating the necessity to carry out intermittent tedious work-ups and time-consuming purifications. Using this TMSOTf-catalyzed one-pot
Stevenson Flemer et al.
Journal of peptide science : an official publication of the European Peptide Society, 18(1), 30-36 (2011-10-29)
A methodology is presented for the facile synthesis of Arg-containing peptides modified at the guanidine headgroup as substituted amidine cores. This process allows for the iterative construction of these Arg isosteres while the peptide is being built out on the
Jean-Louis Brochu et al.
Journal of combinatorial chemistry, 10(3), 405-420 (2008-04-19)
A modular, reagent-based approach to obtain different indoline alkaloid-inspired, tetracyclic architectures is developed. With the use of TBSOTf as a Lewis acid, we report here a tandem Michael-based approach that led to the synthesis of a diastereomeric mixture of tetracyclic
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