Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H21O3P |
| Molecular Weight | 208.235 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)OP(OC(C)C)OC(C)C
InChI
InChIKey=SJHCUXCOGGKFAI-UHFFFAOYSA-N
InChI=1S/C9H21O3P/c1-7(2)10-13(11-8(3)4)12-9(5)6/h7-9H,1-6H3
| Molecular Formula | C9H21O3P |
| Molecular Weight | 208.235 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Mixed N-heterocyclic carbene/phosphite ruthenium complexes: towards a new generation of olefin metathesis catalysts. | 2010-10-14 |
|
| Environmental change in Jiaozhou Bay recorded by nutrient components in sediments. | 2010-09 |
|
| cis-Dichloridobis(triisopropoxy-phosphine)-platinum(II). | 2009-10-17 |
|
| Highly chemoselective copper-catalyzed conjugate reduction of stereochemically labile alpha,beta-unsaturated amino ketones. | 2009-10-02 |
|
| Organocatalytic asymmetric direct phosphonylation of alpha,beta-unsaturated aldehydes: mechanism, scope, and application in synthesis. | 2007-11-09 |
|
| Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria. | 2007-03-21 |
|
| Synthesis of "reversed" methylenecyclopropane analogues of antiviral phosphonates. | 2007 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:29:39 GMT 2025
by
admin
on
Mon Mar 31 22:29:39 GMT 2025
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RJ7QU4YQUN
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