Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H4Cl2O3 |
| Molecular Weight | 170.979 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClCC(=O)OC(=O)CCl
InChI
InChIKey=PNVPNXKRAUBJGW-UHFFFAOYSA-N
InChI=1S/C4H4Cl2O3/c5-1-3(7)9-4(8)2-6/h1-2H2
| Molecular Formula | C4H4Cl2O3 |
| Molecular Weight | 170.979 |
| 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 |
|---|---|---|
| Chemo-enzymatic synthesis of conformationally constrained oligosaccharides. | 2003 Nov 21 |
|
| Combination treatment with Grb7 peptide and Doxorubicin or Trastuzumab (Herceptin) results in cooperative cell growth inhibition in breast cancer cells. | 2007 May 21 |
|
| Cu(II)-catalyzed THM formation during water chlorination and monochloramination: a comparison study. | 2009 Oct 15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:46:02 GMT 2023
by
admin
on
Fri Dec 15 15:46:02 GMT 2023
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| Record UNII |
8Q7TXH7R5F
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| Record Status |
Validated (UNII)
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| Record Version |
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