2,4,6-Trimethyl-2,4,6-trivinylcyclotrisiloxane
Product Information
Molecular Formula
C9H18O3Si3
Molecular Weight
258.49
Description
2,4,6-Trimethyl-2,4,6-trivinylcyclotrisiloxane is a well-known chemical synthesis product that mainly plays an important role in medical research as an important siloxane monomer in elastomer manufacturing. In the biomedical field, applications range from the fabrication of bioactive silicone coatings as an integral part of drug delivery mechanisms.
Synonyms
Cyclotrisiloxane, 2,4,6-triethenyl-2,4,6-trimethyl-; 2,4,6-Triethenyl-2,4,6-trimethylcyclotrisiloxane; Cyclotrisiloxane, 2,4,6-trimethyl-2,4,6-trivinyl-; 2,4,6-Triethenyl-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinane; 2,4,6-Trimethyl-2,4,6-trivinyl-1,3,5,2,4,6-trioxatrisilinane; LS 8170; NSC 242021; Trimethyltrivinylcyclotrisiloxane
IUPAC Name
2,4,6-tris(ethenyl)-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinane
SMILES
C[Si]1(O[Si](O[Si](O1)(C)C=C)(C)C=C)C=C
InChI
InChI=1S/C9H18O3Si3/c1-7-13(4)10-14(5,8-2)12-15(6,9-3)11-13/h7-9H,1-3H2,4-6H3
InChI Key
BVTLTBONLZSBJC-UHFFFAOYSA-N
Boiling Point
80°C
Flash Point
64 °C
Purity
≥95%
Density
0.966 g/cm3
Appearance
Colorless to Almost colorless clear liquid
Related CAS
103202-55-7 (Deleted CAS) 1569492-99-4 (Deleted CAS)
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
3
Exact Mass
258.05637404 g/mol
Monoisotopic Mass
258.05637404 g/mol
Topological Polar Surface Area
27.7Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
243
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-113871708-A | Solid electrolyte and application thereof | 2021-09-26 |
| CN-113336947-A | Fluorosilicone polymer with efficient UV (ultraviolet) photocuring and thermosetting performances, preparation method thereof and coating | 2021-06-24 |
| CN-113388075-A | Composition for 3D printing, 3D printing method and device | 2021-06-11 |
| CN-113150283-A | Fluorosilicone polymer capable of being subjected to UV light and thermal curing, preparation method thereof and coating | 2021-05-10 |
| CN-112876684-A | Micron-level high-crosslinking-degree organic silicon polymer microspheres with controllable particle sizes and preparation method thereof | 2021-03-18 |
| CN-113030295-A | Method for simultaneously determining residual amounts of 21 siloxane compounds in silicone rubber product by gas chromatography-mass spectrometry/mass spectrometry | 2021-02-08 |
| CN-112701255-A | High-temperature-resistant flexible lithium battery positive pole piece and preparation method thereof | 2021-01-27 |
| CN-112759766-A | High-vinyl-activity fluorosilicone rubber raw rubber and preparation method thereof | 2021-01-20 |
| CN-112898573-A | Organic silicon corrosion inhibitor and preparation method thereof | 2021-01-18 |
| CN-112898573-B | Organic silicon corrosion inhibitor and preparation method thereof | 2021-01-18 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 17239899 | 2007-04-01 | Synthesis and applications of novel fluorinated dendrimer-type copolymers by the use of fluoroalkanoyl peroxide as a key intermediate | Journal of colloid and interface science |
