Triethyltin bromide
Product Information
Molecular Formula
C6H15BrSn
Molecular Weight
285.80
Description
Triethyl tin bromide is a clear colorless liquid.
Synonyms
Bromotriethylstannane
IUPAC Name
bromo(triethyl)stannane
SMILES
CC[Sn](CC)(CC)Br
InChI
InChI=1S/3C2H5.BrH.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1
InChI Key
KQPIFPBKXYBDGV-UHFFFAOYSA-M
Boiling Point
223°C at 760 mmHg
Melting Point
-13.5°C
Flash Point
210.2 °F - closed cup
Purity
95%
Density
1.63 g/mL at 25°C(lit.)
Solubility
5 to 10 mg/mL at 72 °F
Appearance
colorless liq.
Refractive Index
n20/D 1.526 (lit.)
Safety Information
Hazards
H300 + H310 + H330 - H410
Precautionary Statement
P262 - P273 - P280 - P301 + P310 + P330 - P302 + P352 + P310 - P304 + P340 + P310
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
285.93792 g/mol
Monoisotopic Mass
285.93792 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
51.3
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113637296-A | Preparation method of polylactic acid composite material and preparation method of degradable optical film | 2021-07-01 |
| KR-20220013066-A | Modified oligomer, modified conjugated diene-based polymer comprising functional group derived from thereof and method for preparing the polymer | 2020-07-24 |
| KR-20220011993-A | Novel compound comprising an imine group, modified conjugated diene-based polymer comprising the compound, method of preparing the polymer and rubber composition comprising the polyemr | 2020-07-22 |
| WO-2022019628-A1 | Novel imine group-containing compound, modified conjugated diene-based polymer comprising same, method for preparing same polymer, and rubber composition comprising same polymer | 2020-07-22 |
| KR-20220007186-A | Novel compound comprising an ester group, modified conjugated diene polymer comprising the compound, method of preparing the polymer and rubber composition comprising the polyemr | 2020-07-10 |
| KR-20210158707-A | Method for preparing modified conjugated diene polymer | 2020-06-24 |
| KR-20210151003-A | Modified conjugated diene polymer, preparing method thereof and rubber composition comprising the same | 2020-06-04 |
| KR-20210147979-A | Method for preparing modified conjugated diene polymer | 2020-05-29 |
| KR-20210145691-A | Preparation method for catalyst composition | 2020-05-25 |
| KR-20210130014-A | Conjugated diene polymer composition, method for preparing the polymer composition and rubber composition comprising the polymer composition | 2020-04-21 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 33929904 | 2021-04-01 | Assessing the Association of Mitochondrial Function and Inflammasome Activation in Murine Macrophages Exposed to Select Mitotoxic Tri-Organotin Compounds | Environmental health perspectives |
| 17632591 | 2007-05-01 | Efficacy of moclobemide in a rat model of neurotoxicant-induced edema | Canadian journal of physiology and pharmacology |
| 16513093 | 2006-04-28 | Organotin compounds enhance 17beta-hydroxysteroid dehydrogenase type I activity in human choriocarcinoma JAr cells: potential promotion of 17beta-estradiol biosynthesis in human placenta | Biochemical pharmacology |
| 15603928 | 2005-02-15 | Some organotin compounds enhance histone acetyltransferase activity | Toxicology letters |
| 7733673 | 1995-04-20 | Cloning and expression of a cDNA for mu-class glutathione S-transferase from rabbit liver | Archives of biochemistry and biophysics |
