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698717

Sigma-Aldrich

聚氧乙基-α-生育酚癸二酸酯

greener alternative

15 wt. % in H2O

别名:

PTS

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About This Item

CAS号:
263015-34-5
分類程式碼代碼:
12162002
NACRES:
NA.22

形狀

liquid

品質等級

100

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

Aligned,

相关类别

一般說明

Learn More at the Professor and Product Portal of Professor Bruce Lipshutz.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced to increase the catalytic efficiency and acts as an environmentally benign and sustainable amphiphile. Click here for more information.

應用

PTS: Amphiphile for Organic Synthesis in Water

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

Zymes LLC 的产品，经美国和世界专利及待审专利独家授权销售。

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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分析证书(COA)

Lot/Batch Number
MKCN9872
MKCL8988
MKCH9292
MKCB6039
MKBZ1035V

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商品

Nok – Third-Generation Amphiphile for Cross-Coupling Chemistry in Water

Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.

Nok – Third-Generation Amphiphile for Cross-Coupling Chemistry in Water

Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.

Baeyer-Villiger Oxidation Reaction

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.

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