Product Name:(3-fluoro-4-(3-morpholinopropoxy)phenyl)boronic acid

IUPAC Name:{3-fluoro-4-[3-(morpholin-4-yl)propoxy]phenyl}boronic acid

CAS:944279-32-7
Molecular Formula:C13H19BFNO4
Purity:95%
Catalog Number:CM219291
Molecular Weight:283.11

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Product Details

CAS NO:944279-32-7
Molecular Formula:C13H19BFNO4
Melting Point:-
Smiles Code:FC1=CC(B(O)O)=CC=C1OCCCN2CCOCC2
Density:
Catalog Number:CM219291
Molecular Weight:283.11
Boiling Point:
MDL No:
Storage:

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.
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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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