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About This Item
Form:
macroporous
form
macroporous
Quality Level
reaction suitability
reaction type: solution phase peptide synthesis, reactivity: proton reactive
extent of labeling
2.5-3.5 mmol/g loading
particle size
40-90 mesh
SMILES string
[O-]C([O-])=O.C=Cc1ccccc1.C=Cc2ccc(C=C)cc2.CC[N+](CC)(CC)Cc3ccccc3.CC[N+](CC)(CC)Cc4ccccc4
InChI
1S/2C13H22N.C10H10.C8H8.CH2O3/c2*1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;1-3-9-5-7-10(4-2)8-6-9;1-2-8-6-4-3-5-7-8;2-1(3)4/h2*7-11H,4-6,12H2,1-3H3;3-8H,1-2H2;2-7H,1H2;(H2,2,3,4)/q2*+1;;;/p-2
InChI key
RBIYTBCFDIQNIC-UHFFFAOYSA-L
Application
Polymer-bound tetraalkylammonium carbonate is a polymer-supported base used for scavenging acidic molecules. It can be used in polymer-assisted solution-phase (PASP) Suzuki reactions.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Polymer-assisted solution-phase (PASP) Suzuki couplings employing an anthracene-tagged palladium catalyst.
Lan P, et al.
The Journal of Organic Chemistry, 68(25), 9678-9686 (2003)
S R Stauffer et al.
Journal of combinatorial chemistry, 2(4), 318-329 (2000-07-13)
Most ligands for the estrogen receptor (ER) are not well suited for synthesis by combinatorial means, because their construction involves a series of carbon-carbon bond forming reactions that are not uniformly high yielding. In previous work directed to overcoming this
Recent applications of polymer-supported reagents and scavengers in combinatorial, parallel, or multistep synthesis.
Thompson L A.
Current Opinion in Chemical Biology, 4(3), 324-337 (2000)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 540293-5G | 04061832945835 |
| 540293-25G | 04061832945828 |