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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)-

Butanoic acid, 4,4'-(1,1,3,3-tetramethyl-1,3-disiloxanediyl)bis-

OC(=O)CCC[Si](O[Si](CCCC(=O)O)(C)C)(C)C Request for Quotation
Chemical Name: Butanoic acid, 4,4'-(1,1,3,3-tetramethyl-1,3-disiloxanediyl)bis-
CAS Number: 3353-68-2
Product Number: AG00C0IV(AGN-PC-0JLQBT)
Synonyms:
MDL No:
Molecular Formula: C12H26O5Si2
Molecular Weight: 306.5028

Identification/Properties

Computed Properties
Molecular Weight:
306.505g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
10
Exact Mass:
306.132g/mol
Monoisotopic Mass:
306.132g/mol
Topological Polar Surface Area:
83.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
285
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4,4'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)dibutanoic acid is a versatile chemical compound widely used in chemical synthesis processes. With its unique molecular structure, this acid plays a crucial role in several key applications within the field of chemistry.One notable application of this compound is its use as a linking agent in the synthesis of novel polymers. By incorporating 4,4'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)dibutanoic acid into polymer chains, researchers can tailor the physical and chemical properties of the resulting material. This allows for the creation of new materials with specific functionalities and characteristics, making it invaluable in the development of advanced materials for various industries.Furthermore, this acid can also serve as a coupling agent in organic synthesis reactions. Its ability to form stable bonds between different functional groups enables chemists to efficiently connect molecular components, facilitating the synthesis of complex organic molecules. This application is particularly valuable in the pharmaceutical industry, where precise control over molecular structure is essential for drug development.In addition, the 4,4'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)dibutanoic acid is utilized as a protecting group in organic chemistry reactions. By selectively shielding reactive functional groups with this compound, chemists can control the reactivity of specific sites within a molecule, allowing for the sequential modification of complex compounds with precision. This protective function is vital in multi-step organic synthesis processes, where the preservation of specific chemical moieties is essential to the overall reaction scheme.Overall, the 4,4'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)dibutanoic acid proves to be a versatile and indispensable tool in chemical synthesis, enabling the development of novel materials, the synthesis of complex molecules, and the precise manipulation of chemical reactions.