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Product Name:(3-Fluoro-5-(morpholine-4-carbonyl)-phenyl)boronic acid

IUPAC Name:[3-fluoro-5-(morpholine-4-carbonyl)phenyl]boronic acid

CAS:874219-40-6
Molecular Formula:C11H13BFNO4
Purity:98%
Catalog Number:CM137249
Molecular Weight:253.04

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Product Details

CAS NO:874219-40-6
Molecular Formula:C11H13BFNO4
Melting Point:-
Smiles Code:OB(O)C1=CC(F)=CC(=C1)C(=O)N1CCOCC1
Density:
Catalog Number:CM137249
Molecular Weight:253.04
Boiling Point:
MDL No:MFCD08235057
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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