Название продукции:Potassium trifluoro(1H-indol-5-yl)borate
IUPAC Name:potassium trifluoro(1H-indol-5-yl)boranuide
- CAS：1111733-03-9
- Молекулярная формула：C8H6BF3KN
- Чистота：95%+
- Номер в каталоге：CM234394
- Молекулярная масса：223.05
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Информация о продукции
- Номер CAS:1111733-03-9
- Молекулярная формула:C8H6BF3KN
- Точка плавления:-
- Smiles-код:F[B-](F)(C1=CC2=C(NC=C2)C=C1)F.[K+]
- Плотность:
- Номер в каталоге:CM234394
- Молекулярная масса:223.05
- Точка кипения:
- Номер Mdl:
- Хранение:
Category Infos
- Indoles
- Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.
- indole company
- As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.
- 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.
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