cas 1268340-93-7|| where to buy trifluoro(piperidin-1-ium-1-ylmethyl)boranuide

Nom du produit:trifluoro(piperidin-1-ium-1-ylmethyl)boranuide

IUPAC Name:trifluoro[(piperidin-1-ium-1-yl)methyl]boranuide

Unité d'emballage	Stock disponible	Prix($)
CM180230-1g	in stock	ƦȺ
CM180230-5g	in stock	Ⱥŵǜ

Pour une utilisation en R&D uniquement..

Formulaire de demande

Nom chimique

Numéro CAS

Quantité*

Spécifications requises*
(% d'analyse, qualité du matériau, etc.)

Nom du contact*

Email du contact*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 1268340-93-7 regularly via the above email.

Notes supplémentaires

Verification code*

refresh

: N° CAS:1268340-93-7; Formule moléculaire:C6H13BF3N; Point de fusion:-; Code SMILES:F[B-](F)(C[NH+]1CCCCC1)F; Densité:

: Numéro de catalogue:CM180230; Poids moléculaire:166.98; Point d'ébullition:; N° Mdl:MFCD18071160; Stockage:Store at 2-8°C.

: 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.; Piperidine,Piperidine Price; if you want to know the latest news about piperidine and piperidine price, please come to our website and get a quote for free.

: Borates; Borates are classified as critical materials, they are the main source of boron and have a variety of industrial applications. Organic trifluoroborate is stable to heat, air and humidity, and is a very convenient crystalline boric acid compound. Since it has a tetra-coordinated boronic acid structure after the substitution of fluorine, it does not exhibit Lewis acidity and is stable to oxidation conditions. In addition, it can be regarded as the protector of boronic acid and boronic acid ester, which can be converted into each other. The compound can generally exist stably in organic solvents, but will decompose in protic solvents to liberate trivalent boron, so it can be directly used as a substrate for Suzuki coupling. The difference between trifluoroborate and boric acid is that it must exist in a monomeric form, so the equivalent weight can be closely controlled.