2,2-Dibutyl-1,3,2-dioxastannolane
Product Information
Molecular Formula
C10H22O2Sn
Molecular Weight
292.99
Description
2,2-Dibutyl-1,3,2-dioxastannolane is an extraordinary biomedical compound extensively utilized in the realm of biomedicine owing to its inherent attributes as a prospective antineoplastic agent. Displaying distinctiveness in both its structure and properties, this compound exhibits considerable potential in combatting a multitude of cancer variants by impeding the proliferation of tumors and triggering programmed cell death. Hence, it harbors immense promise for advancement in the sphere of cancer investigations and therapeutic interventions.
Synonyms
2,2-Dibutyl-[1,3,2]dioxastannolane; 1,1-dibutylstanna-2,5-dioxacyclopentane; 1-di-n-butyl-1-stanna-2,5-dioxacyclopentane; 2,2-Dibutyl-[1,3,2]dioxastannolane, 96%
IUPAC Name
2,2-dibutyl-1,3,2-dioxastannolane
SMILES
CCCC[Sn]1(OCCO1)CCCC
InChI
InChI=1S/2C4H9.C2H4O2.Sn/c2*1-3-4-23-1-2-4/h2*1,3-4H2,2H31-2H2/q-2+2
InChI Key
STWBEJNHFFEKHC-UHFFFAOYSA-N
Melting Point
231-236 °C
Purity
96%
Safety Information
Hazards
H300
Precautionary Statement
P264-P301 + P310
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
6
Exact Mass
294.064182 g/mol
Monoisotopic Mass
294.064182 g/mol
Topological Polar Surface Area
18.5Ų
Heavy Atom Count
13
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 |
|---|---|---|
| JP-2021120372-A | Nebivolol synthesis method and its intermediate compounds | 2019-09-05 |
| KR-101711636-B1 | Room Temperature Cross linking Type, Halogen-free Flame Retardant Composition and manufacturing method thereof | 2015-08-25 |
| US-10174187-B2 | Room temperature crosslinked type halogen-free flame retardant resin composition, and method of preparing the same | 2015-08-25 |
| US-2017058113-A1 | Room temperature crosslinked type halogen-free flame retardant resin composition, and method of preparing the same | 2015-08-25 |
| EP-3299364-A1 | Nebivolol synthesis method and intermediate compound thereof | 2015-05-19 |
| JP-2018522060-A | Nebivolol synthesis method and intermediate compounds thereof | 2015-05-19 |
| JP-2020019774-A | Synthetic method of nebivolol and intermediate compound thereof | 2015-05-19 |
| US-10526304-B2 | Nebivolol synthesis method and intermediate compound thereof | 2015-05-19 |
| US-2018141926-A1 | Nebivolol synthesis method and intermediate compound thereof | 2015-05-19 |
| US-2020102282-A1 | Nebivolol synthesis method and intermediate compound thereof | 2015-05-19 |
