-
-
-
45993-250MGThis substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here Application Refer to the product′s
-
47745-UStyrene is a volatile compound, used in the manufacture of numerous types of plastic, glass fiber-reinforced resins, protective coatings, synthetic rubber and ion exchange resins. Application Refer to the product′s Certificate of Analysis for
-
702730-100MLApplication tert -Butylchlorodiphenylsilane can be used to prepare 1-benzyloxy-3-( tert -butyldiphenylsilyloxy)propan-2-ol, a key intermediate for the synthesis of mono- O -protected pyrimidine acyclic nucleosides.
-
495492-25ML
Sigma-Aldrich
tert-Butyldimethyl(2-propynyloxy)silane (C15-1280-249)
Price: $460.65List Price: $511.84tert -Butyldimethyl(2-propynyloxy)silane is an aliphatic terminal alkyne. Application tert -Butyldimethyl(2-propynyloxy)silane may be used in the synthesis of ( R )-2,3-pentadecadien-1-ol and ( S )-ethyl 5-( tert -
495492-5ML
Sigma-Aldrich
tert-Butyldimethyl(2-propynyloxy)silane (C15-1280-250)
Price: $169.67List Price: $188.52tert -Butyldimethyl(2-propynyloxy)silane is an aliphatic terminal alkyne. Application tert -Butyldimethyl(2-propynyloxy)silane may be used in the synthesis of ( R )-2,3-pentadecadien-1-ol and ( S )-ethyl 5-( tert -
376213-25MLTrimethoxy(octadecyl)silane (OTMS) is an alkyl silane that functionalizes a variety of nanoparticle surfaces and facilitates a hydrophobic coating with a high-water contact angle and low surface energy. Trimethoxy(octadecyl)silane (OTS) is an
-
376213-5MLTrimethoxy(octadecyl)silane (OTMS) is an alkyl silane that functionalizes a variety of nanoparticle surfaces and facilitates a hydrophobic coating with a high-water contact angle and low surface energy. Trimethoxy(octadecyl)silane (OTS) is an
-
111406-25GVinylcyclohexane
-
111406-5GVinylcyclohexane
-
213950-100GApplication Used for the preparation of trimethylsilylethyl sulfoxides which in the presence of fluoride ion generate sulfenate nucleophiles.