cas 1451391-92-6|| where to buy Lithium trimethoxy(thiazol-2-yl)borate

Название продукции:Lithium trimethoxy(thiazol-2-yl)borate

IUPAC Name:lithium(1+) trimethoxy(1,3-thiazol-2-yl)boranuide

: CAS：1451391-92-6; Молекулярная формула：C6H11BLiNO3S; Чистота：95%

Упаковочная единица	Доступно для заказа	Цена ($)	Количество
CM189861-1g	1-2 Weeks	ưȐǜ

Только для использования в НИОКР..

Форма запроса

Химическое название

Номер CAS

Количество*

Необходимые спецификации*
(% пробы, категория материала и т.д.)

Контактное лицо*

Электронная почта*

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 1451391-92-6 regularly via the above email.

Дополнительные примечания

Verification code*

refresh

: Номер CAS:1451391-92-6; Молекулярная формула:C6H11BLiNO3S; Точка плавления:-; Smiles-код:CO[B-](OC)(OC)C1=NC=CS1.[Li+]; Плотность:

: Номер в каталоге:CM189861; Молекулярная масса:194.97; Точка кипения:; Номер Mdl:MFCD26131440; Хранение:

: Thiazoles; Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.

: 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.