|Related Categories||Bases, Chemical Synthesis, Organic Bases, Solid Supported Synthesis, Specialty Synthesis,|
|crosslinking||2 % cross-linked with divinylbenzene|
|extent of labeling||2.6 mmol/g loading|
|particle size||200-400 mesh|
1, 5, 25 g in glass bottle
This versatile polymer-bound base has been used as a reusable basic catalyst foe regioselective acylations; as both a base for the deprotonation of phenols and as a scavenger of excess phenil in the synthesis of aryl ethers from phenols; in the addition of dialkyl phosphites to a variety of carbonyl compounds, as well as, serving as a catalyst in the nitroaldol (Henry) reaction; and as a scavenger of activated ester electophiles.
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purum, ≥98.0% (T)
extent of labeling: ~2.6 mmol/g base loading
100-200 mesh, extent of labeling: 1.15 mmol N per g loading, 1 % cross-linked with divinylbenzene
100-200 mesh, extent of labeling: 2.3 mmol/g loading, 1 % cross-linked
Certificate of Analysis
|Precautionary statements||P280-P305 + P351 + P338-P310|
|Personal Protective Equipment||Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges|
|Hazard Codes (Europe)||C|
|Risk Statements (Europe)||34|
|Safety Statements (Europe)||26-36/37/39-45|
|RIDADR||UN 3263 8 / PGII|
Tamura, Y. Synth. Commun. 24, 2907, (1994)
Xu, W. et. al. Tetrahedron Lett. 38, 7337, (1997)
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