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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)-

Silanediol, dimethyl-, diacetate

C[Si](O)(O)C.CC(=O)O.CC(=O)O Request for Quotation
Chemical Name: Silanediol, dimethyl-, diacetate
CAS Number: 2182-66-3
Product Number: AG003PAU(AGN-PC-0O7WME)
Synonyms:
MDL No:
Molecular Formula: C6H16O6Si
Molecular Weight: 212.27314

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
176.243g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
176.05g/mol
Monoisotopic Mass:
176.05g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
157
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:
Danger
UN#:
3265
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Dimethylsilanediyl diacetate is a valuable reagent in chemical synthesis due to its ability to serve as a versatile precursor in various reactions. This compound is commonly used in the synthesis of silicon-containing polymers and materials, as well as in the preparation of organosilicon compounds with diverse properties. Its unique structure allows for selective functionalization and modification of silicon atoms, enabling the creation of tailored molecules for specific applications in industry and research. Additionally, Dimethylsilanediyl diacetate can facilitate the formation of silicon-based coatings, adhesives, and sealants, showcasing its utility in the production of advanced materials with enhanced performance characteristics. Furthermore, its compatibility with different types of reactions and functional groups makes it a valuable tool for organic and inorganic chemistry alike, offering opportunities for innovation and discovery in the field of materials science.