Chemical Name:N,O-Bis(trimethylsilyl)acetamide
It involves demanding processes including high pressure hydrogenation, oxygen free water environment, ultra low temperature environment and highly corrosive environmentIn addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.The target product of synthetic weights ranging from milligrams to kilograms. We have successfully completed a large number of orders for chemical custom synthesis on timeWe are a market leader in the development and manufacturing of high performance specialty chemicals. We foster an ambitious culture that focuses on open innovation for new chemical products and business growth.With strong technical accumulation and innovative research and development capabilities, he is good at various types of chemical reactions such as hydrogenation, nitration, Suzuki coupling, cyanation, diazotization, bromination, wittig reaction, Grignard reaction, redox reaction and ultra-low temperature reaction.
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CAS.NO:10416-59-8
Synonyms:BSA
Molecular Formula:C8H21NOSi2
Molecular Weight:203.42900
Physical and Chemical Properties:
Density:0.832;
Melting point:24oC;
Boiling point:71-73oC;
Flash point:42oC;
Index of Refraction:1.417;
Specification:
Appearance:Clear to yellowish clear liquid
Purity(GC):≥98.0%
Packing:25 kg/drum, can also be packaged according to customer requirements
Storage:Store in a cool, ventilated place
Application:The trimethylsilyl group is a frequently utlized monofunctional blocking group for protic organic and inorganic materials.
As the product eliminated during the silylation is neutral acetamide, it can be preferably used for substrates which are acid-or base-sensitive.
It can be used for blocking and protection of hydroxyl groups in natural products,e.g. amino acids, carbohydrates.
It can be used for blocking and protection of functional groups in organic intermediates.
The silylated derivatives show improved chemical stability than the original compounds and allow chemical reactions which otherwise would not be possible.
It can be used for formation of derivatives of H-acid compounds for analysis.
The silylated derivatives are volatile and can therefore be determined by gas chromatography.