Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
推薦產品
形狀
liquid
分子量
~1,200
反應適用性
reaction type: C-C Bond Formation
環保替代產品特色
Waste Prevention
Designing Safer Chemicals
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
濃度
15 wt. % in H2O
環保替代類別
一般說明
應用
Uses:
- Provides an aqueous micellar environment for transition metal-catalyzed Heck coupling, cross metathesis and ring closing metathesis reactions
- Surfactant for catalytic asymmetric Baeyer-Villiger oxidation in water using PtII catalysts and hydrogen peroxide
- Orally active CoQ10 carrier for neuroprotection after stroke or cardiac arrest
法律資訊
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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文章
Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.
Surfactants for efficient reactions in water as a green chemistry alternative.
Baeyer-Villiger 氧化作用是氧化裂解與羰基相鄰的碳-碳鍵,將酮類轉換為酯類,環酮類轉換為內酯類。
The Baeyer-Villiger oxidation is the oxidative cleavage of a carbon-carbon bond adjacent to a carbonyl, which converts the ketones to esters and the cyclic ketones to lactones.
相關內容
Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.
Designer surfactants enable diverse transformations like Suzuki-Miyaura, Olefin Metathesis, and 1,4-Addition to Enones in water by Prof. Bruce Lipshutz.
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What is the Department of Transportation shipping information for this product?
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What can Product 698717, Polyoxyethanyl-α-tocopheryl sebacate, be used for?
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PTS is a non-ionic amphiphile that can be used to "solubilize" organic molecules in aqueous media. The PTS molecule forms micelles around the lipophilic compounds, allowing them to move into the aqueous phase for effective cross-coupling and metathesis reactions without the need of a co-solvent.
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