Название продукции:4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)thiomorpholine 1,1-dioxide

IUPAC Name:4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}-1λ⁶-thiomorpholine-1,1-dione

CAS:1092563-25-1
Молекулярная формула:C17H26BNO4S
Чистота:95%
Номер в каталоге:CM204812
Молекулярная масса:351.27

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Информация о продукции

Номер CAS:1092563-25-1
Молекулярная формула:C17H26BNO4S
Точка плавления:-
Smiles-код:CC1(C)C(C)(C)OB(C2=CC=C(C=C2)CN3CCS(CC3)(=O)=O)O1
Плотность:
Номер в каталоге:CM204812
Молекулярная масса:351.27
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

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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Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.
Thiomorpholines
Thiomorpholine is a nitrogen- and sulfur-containing heterocyclic compound with the molecular formula C4H9NS. It can be considered a thio analog of morpholine. Thiomorpholines are comparable to other secondary amines in terms of nucleophilicity and N-alkylation or acylation with alkyl groups or acid halides.

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