493813
Morpholine, polymer-bound
200-400 mesh, extent of labeling: 2.75-3.25 mmol/g loading, 1 % cross-linked
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N-Vinylbenzylmorpholine-divinylbenzene copolymer
C29H33NO
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Quality Level
crosslinking
1 % cross-linked
reaction suitability
reaction type: solution phase peptide synthesis
reactivity: proton reactive
extent of labeling
2.75-3.25 mmol/g loading
particle size
200-400 mesh
InChI
1S/C4H9NO/c1-3-6-4-2-5-1/h5H,1-4H2
InChI key
YNAVUWVOSKDBBP-UHFFFAOYSA-N
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Related Categories
Application
This polymer-bound tertiary amine is used as a base in the synthesis of sulfonamides and amides, serves as a catalyst in the functionalization of secondary amines, with acid chlorides. The resin was also used as a polymer-bound base to scavenge excess acid.
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Tetrahedron Letters, 39, 3635-3635 (1998)
Tetrahedron, 54, 3983-3983 (1998)
Journal of the American Chemical Society, 119, 4882-4882 (1997)
The Journal of antimicrobial chemotherapy, 70(1), 14-22 (2014-09-11)
Antifungal prescription remains a challenge in pregnant women because of uncertainties regarding fetal toxicity and altered maternal pharmacokinetic parameters that may affect efficacy or increase maternal and fetal toxicity. We present updated data reviewing the available knowledge and current recommendations
Physical chemistry chemical physics : PCCP, 17(29), 19474-19483 (2015-07-07)
A new series of ester functionalized cationic gemini surfactants having different cationic headgroups (i.e. piperidinium, pyrrolidinium, morpholinium and quaternary ammonium) have been synthesized and characterized using NMR and Mass spectroscopy. These new gemini surfactants were investigated for their micellization and
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