TRIBUTYL(3-METHYL-2-BUTENYL)TIN
Product Information
Molecular Formula
C17H36Sn
Molecular Weight
359.18
Description
TRIBUTYL(3-METHYL-2-BUTENYL)TIN presents promising prospects in combating an array of diseases, encompassing specific cancer variants and fungal afflictions. By virtue of its distinctive configuration, this compound intricately interacts with targeted receptors, thereby bestowing an array of auspicious therapeutic advantages.
Synonyms
DIMETHYLALLYLTRIBUTYLSTANNANE; 3-METHYL-2-BUTENYLTRIBUTYLSTANNANE; PRENYLSTANNANE; TRIBUTYL(3-METHYL-2-BUTENYL)TIN; TRIBUTYL(3-METHYL-2-BUTENYL)TIN(IV); TRI-N-BUTYL(3-METHYL-2-BUTENYL)TIN; 3,3-Dimethylallyl(tri-n-butyl)tin~Prenyl(tri-n-butyl)stannane; Tributyl-
IUPAC Name
tributyl(3-methylbut-2-enyl)stannane
SMILES
CCCC[Sn](CCCC)(CCCC)CC=C(C)C
InChI
InChI=1S/C5H9.3C4H9.Sn/c1-4-5(2)33*1-3-4-2/h4H,1H2,2-3H33*1,3-4H2,2H3
InChI Key
XEFRYQPTIWSVGI-UHFFFAOYSA-N
Boiling Point
283 °C (lit.)
Purity
90%
Density
1.069
Refractive Index
n20/D 1.488 (lit.)
Safety Information
Hazards
H301-H312-H315-H319-H372-H410
Precautionary Statement
P273-P280-P301 + P310-P305 + P351 + P338-P314-P501
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
11
Exact Mass
360.183904 g/mol
Monoisotopic Mass
360.183904 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
192
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-108929334-B | Preparation method of morpholine dione natural alkaloid and derivative thereof | 2018-07-16 |
| EP-3389380-A1 | Spirocyclic quinolizine derivatives useful as hiv integrase inhibitors | 2015-12-15 |
| US-10544155-B2 | Spirocyclic quinolizine derivatives useful as HIV integrase inhibitors | 2015-12-15 |
| US-2019040076-A1 | Spirocyclic Quinolizine Derivatives Useful as HIV Integrase Inhibitors | 2015-12-15 |
| WO-2017106071-A1 | Spirocyclic quinolizine derivatives useful as hiv integrase inhibitors | 2015-12-15 |
| EP-3389380-B1 | Spirocyclic quinolizine derivatives useful as hiv integrase inhibitors | 2015-12-15 |
| WO-2014022377-A1 | Membranes and coatings made from mixtures including ionic liquids having silicon-bonded hydrolyzable groups | 2012-07-30 |
| US-2014178761-A1 | Fabrication method for metal battery electrode with pyrolyzed coating | 2012-03-28 |
| US-2017149053-A1 | Battery electrode with metal particles and pyrolyzed coating | 2012-03-28 |
| US-9627671-B2 | Fabrication method for metal battery electrode with pyrolyzed coating | 2012-03-28 |
