Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10Cl2Sn |
| Molecular Weight | 343.824 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl[Sn](Cl)(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=ISXUHJXWYNONDI-UHFFFAOYSA-L
InChI=1S/2C6H5.2ClH.Sn/c2*1-2-4-6-5-3-1;;;/h2*1-5H;2*1H;/q;;;;+2/p-2
| Molecular Formula | C12H10Cl2Sn |
| Molecular Weight | 343.824 |
| 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 |
|---|---|---|
| Identification of inhibitors of drug-resistant Candida albicans strains from a library of bicyclic peptidomimetic compounds. | 2010-03-25 |
|
| Synthesis, characterization and biocidal activity of new organotin complexes of 2-(3-oxocyclohex-1-enyl)benzoic acid. | 2010-03 |
|
| Structure-dependent activation of peroxisome proliferator-activated receptor (PPAR) gamma by organotin compounds. | 2009-07-15 |
|
| Trialkyltin compounds bind retinoid X receptor to alter human placental endocrine functions. | 2005-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:53:21 GMT 2025
by
admin
on
Mon Mar 31 19:53:21 GMT 2025
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| Record UNII |
0Y7MZ4K0DR
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| Record Status |
Validated (UNII)
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