Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H4Cl2O2 |
| Molecular Weight | 203.022 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(=O)C1=CC=CC=C1C(Cl)=O
InChI
InChIKey=FYXKZNLBZKRYSS-UHFFFAOYSA-N
InChI=1S/C8H4Cl2O2/c9-7(11)5-3-1-2-4-6(5)8(10)12/h1-4H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Hydrolytic stability of terephthaloyl chloride and isophthaloyl chloride. | 2006-10-15 |
|
| Stereoselective alpha-fluoroamide and alpha-fluoro-gamma-lactone synthesis by an asymmetric zwitterionic aza-Claisen rearrangement. | 2005-10-17 |
|
| Highly active, regioselective, and enantioselective hydroformylation with Rh catalysts ligated by Bis-3,4-diazaphospholanes. | 2005-04-13 |
|
| Reverse thermo-responsive poly(ethylene oxide) and poly(propylene oxide) multiblock copolymers. | 2005-02 |
|
| Resolved chiral 3,4-diazaphospholanes and their application to catalytic asymmetric allylic alkylation. | 2003-10-01 |
|
| Atomic force microscopy imaging of novel type of polymeric colloidal nanostructures. | 2002-11 |
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8S64APH24W
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Phthaloyl chloride
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6955
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DTXSID8038691
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88-95-9
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m8757
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44611
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201-869-0
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SUBSTANCE RECORD