Nom du produit:potassium trifluoro(3-morpholino-3-oxopropyl)borate
IUPAC Name:potassium trifluoro[3-(morpholin-4-yl)-3-oxopropyl]boranuide
- CAS：1150654-74-2
- Formule moléculaire：C7H12BF3KNO2
- Pureté：95%
- Numéro de catalogue：CM279994
- Poids moléculaire：249.08
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1150654-74-2
- Formule moléculaire:C7H12BF3KNO2
- Point de fusion:-
- Code SMILES:O=C(N1CCOCC1)CC[B-](F)(F)F.[K+]
- Densité:
- Numéro de catalogue:CM279994
- Poids moléculaire:249.08
- Point d'ébullition:
- N° Mdl:MFCD10700166
- Stockage:
Category Infos
- Morpholines
- Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
- morpholine price
- if you are interested in morpholine price, please feel free to contact us. More information of our products will be forwarded to you upon receipt of your specific inquiry.
- 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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