Название продукции:dicyclopentyldimethoxysilane

IUPAC Name:dicyclopentyldimethoxysilane

CAS:126990-35-0
Молекулярная формула:C12H24O2Si
Чистота:98%
Номер в каталоге:CM138152
Молекулярная масса:228.41

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Информация о продукции

Номер CAS:126990-35-0
Молекулярная формула:C12H24O2Si
Точка плавления:-
Smiles-код:CO[Si](C1CCCC1)(C2CCCC2)OC
Плотность:
Номер в каталоге:CM138152
Молекулярная масса:228.41
Точка кипения:251°C at 760 mmHg
Номер Mdl:MFCD01074471
Хранение:Store at 2-8°C.

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Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Cyclopentanes
Cyclopentane is a cycloalkane, an organic compound with a molecular formula of C5H10, a colorless and transparent liquid, insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, carbon tetrachloride, acetone, etc. It is mainly used as a solvent and chromatographic reference materials.
Cyclopentanes,where to buy Cyclopentanes
Cyclopentanes
Cyclopentane (also called C pentane) is a highly flammable alicyclic hydrocarbon with chemical formula C5H10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It occurs as a colorless liquid with a petrol-like odor.

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Silane Compounds
Silanes are a series of silicon substitutes for carbon alkanes, which consisting of multiple silicon atoms linked to each other as the main chain and hydrogen atoms or other chemical elements linked with the main chain. Silanes are versatile chemicals used in the modification of SPR sensor surfaces. In particular, the silane molecules, such as 3-mercaptopropyl trimethoxy silane, are convenient for use as linkers in surface modification of SPR sensors.

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