Product Name:(2-(Piperidin-1-yl)phenyl)boronic acid

IUPAC Name:[2-(piperidin-1-yl)phenyl]boronic acid

CAS:1050505-85-5
Molecular Formula:C11H16BNO2
Purity:95%+
Catalog Number:CM135403
Molecular Weight:205.06

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CM135403-5g in stock ƿȃŹ

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Product Details

CAS NO:1050505-85-5
Molecular Formula:C11H16BNO2
Melting Point:-
Smiles Code:OB(O)C1=C(C=CC=C1)N1CCCCC1
Density:
Catalog Number:CM135403
Molecular Weight:205.06
Boiling Point:391.6°C at 760 mmHg
MDL No:MFCD03095111
Storage:Keep in a tight container and store at 2°C~8°C

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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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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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.

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