Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H15BrSn |
| Molecular Weight | 285.797 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[Sn](Br)(CC)CC
InChI
InChIKey=KQPIFPBKXYBDGV-UHFFFAOYSA-M
InChI=1S/3C2H5.BrH.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1
| Molecular Formula | C6H15BrSn |
| Molecular Weight | 285.797 |
| 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 |
|---|---|---|
| Cloning and expression of a cDNA for mu-class glutathione S-transferase from rabbit liver. | 1995 Apr 20 |
|
| Some organotin compounds enhance histone acetyltransferase activity. | 2005 Feb 15 |
|
| Organotin compounds enhance 17beta-hydroxysteroid dehydrogenase type I activity in human choriocarcinoma JAr cells: potential promotion of 17beta-estradiol biosynthesis in human placenta. | 2006 Apr 28 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:10:02 GMT 2023
by
admin
on
Fri Dec 15 19:10:02 GMT 2023
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| Record UNII |
UOP17166KC
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| Record Status |
Validated (UNII)
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| Record Version |
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EPA PESTICIDE CODE |
683112
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2767-54-6
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UOP17166KC
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220-443-5
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DTXSID9040712
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17701
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