Stannane,dichlorobis(1,1-dimethylethyl)-
Product Information
Molecular Formula
C8H18 Cl2 Sn
Molecular Weight
303.84
Description
Microbial bifunctional peptidases, like Stannane,dichlorobis(1,1-dimethylethyl)-, have garnered significant interest in therapeutics due to their versatile potential. This biomedical marvel serves as a pivotal intermediate for drug synthesis, both in pharmaceutical and agrochemical domains. By precisely modulating enzymatic activities and receptor engagements, this compound exhibits immense promise in combatting multifarious ailments like cancer, diabetes, and cardiovascular disorders.
Synonyms
DI-T-BUTYLTIN DICHLORIDE; DI-T-BUTYLDICHLOROTIN; DI-TERT-BUTYLTIN DICHLORIDE; di-tert-butyldichlorostannane; DI-TERT-BUTYLDICHLOROTIN; Di-t-butyltindichloride,98%; DI-TERT-BUTYLTINCHLORIDE; Di-tert-B-butyltin dichloride, 98%
IUPAC Name
ditert-butyl(dichloro)stannane
SMILES
CC(C)(C)[Sn](C(C)(C)C)(Cl)Cl
InChI
InChI=1S/2C4H9.2ClH.Sn/c2*1-4(2)3/h2*1-3H32*1H/q+2/p-2
InChI Key
PEGCFRJASNUIPX-UHFFFAOYSA-L
Boiling Point
66 °C/3 mmHg (lit.)
Melting Point
40-42 °C (lit.)
Flash Point
235.4 °F - closed cup
Purity
98%
Safety Information
Hazards
H301 + H311 + H331 - H314
Precautionary Statement
P260 - P280 - P301 + P310 + P330 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
2
Exact Mass
303.980759 g/mol
Monoisotopic Mass
303.980759 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
123
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 |
|---|---|---|
| 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 |
| CN-113831238-A | Method for preparing methyl lactate by catalytic conversion of carbohydrate | 2020-06-24 |
| 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 |
