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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3,7-Dioxa-2,8-disilanonane, 2,2,8,8-tetramethyl-

C[Si](OCCCO[Si](C)(C)C)(C)C Request for Quotation
Chemical Name: 3,7-Dioxa-2,8-disilanonane, 2,2,8,8-tetramethyl-
CAS Number: 17887-80-8
Product Number: AG0026F9(AGN-PC-0JMR92)
Synonyms:
MDL No:
Molecular Formula: C9H24O2Si2
Molecular Weight: 220.4567

Identification/Properties

Properties
BP:
199.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
220.459g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
6
Exact Mass:
220.131g/mol
Monoisotopic Mass:
220.131g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
120
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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H227-H315-H319
Precautionary Statements:
P210-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P370+P378-P403+P235-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2,8,8-Tetramethyl-3,7-dioxa-2,8-disilanonane is a versatile compound widely utilized in chemical synthesis due to its unique properties. In the realm of organic chemistry, this compound serves as an important building block in the creation of various silicon-containing molecules. Its branched structure and silicone backbone make it an ideal precursor for the synthesis of complex organosilicon compounds with diverse applications.One key application of 2,2,8,8-Tetramethyl-3,7-dioxa-2,8-disilanonane lies in the formation of silicon-based polymers. By utilizing this compound as a starting material, chemists can tailor the properties of the resulting polymers, such as thermal stability, flexibility, and hydrophobicity. These silicone polymers find use in a wide range of industrial applications, including coatings, adhesives, and lubricants.Furthermore, 2,2,8,8-Tetramethyl-3,7-dioxa-2,8-disilanonane can also be employed in the synthesis of novel organosilicon compounds for pharmaceutical and electronic applications. Its ability to introduce silicon moieties into organic molecules allows for the development of new materials with enhanced properties, paving the way for advancements in various industries.Overall, the strategic use of 2,2,8,8-Tetramethyl-3,7-dioxa-2,8-disilanonane in chemical synthesis opens up avenues for the creation of innovative silicon-containing compounds with tailored functionalities, benefiting diverse fields of science and technology.