4,4'-Bis(triethoxysilyl)-1,1'-biphenyl - 123640-93-7

4,4'-Bis(triethoxysilyl)-1,1'-biphenyl

Catalog Number: EVT-351291
CAS Number: 123640-93-7
Molecular Formula: C24H38O6Si2
Molecular Weight: 478.7 g/mol
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Product Introduction

Description

The compound 4,4'-Bis(triethoxysilyl)-1,1'-biphenyl is a chemical of interest due to its potential applications in various fields. While the provided data does not directly discuss this compound, it does include information on structurally related compounds that can offer insights into the behavior and applications of bis-silylated biphenyls. For instance, compounds with bis-silyl groups, such as bis[3-(triethoxysilyl)propyl]tetrasulfide, have been utilized in the synthesis of phosphorothioates, indicating the utility of silyl groups in synthetic chemistry3.

Mechanism of Action

The mechanism of action for 4,4'-Bis(triethoxysilyl)-1,1'-biphenyl is not explicitly detailed in the provided papers. However, we can infer from related compounds that the presence of silyl groups can confer unique properties. For example, bis[3-(triethoxysilyl)propyl]tetrasulfide acts as a sulfur-transferring agent in the synthesis of nucleoside phosphorothioates, suggesting that silyl groups can facilitate the transfer of functional groups in synthetic processes3. Additionally, compounds with bis(diethylaminoethoxy) groups have been shown to inhibit lysosomal phospholipases, which could imply that bis-silylated compounds might interact with biological molecules in a similar fashion, although the exact mechanism would likely differ due to the distinct chemical nature of the silyl groups1.

Applications in Various Fields

The applications of 4,4'-Bis(triethoxysilyl)-1,1'-biphenyl can be diverse, as suggested by the applications of structurally related compounds. For instance, bis[3-(triethoxysilyl)propyl]tetrasulfide is used in the synthesis of phosphorothioate oligonucleotides, which are important in molecular biology and therapeutic applications3. This indicates that bis-silylated biphenyls could potentially be used in the synthesis of biologically relevant molecules. Moreover, the inhibition of lysosomal enzymes by related compounds suggests potential applications in the study of lysosomal storage diseases or the development of therapeutic agents1. Lastly, the versatility of compounds like 2-phenyl-4-bis(methylthio)methyleneoxazol-5-one in synthesizing heterocyclic scaffolds hints at the possibility of 4,4'-Bis(triethoxysilyl)-1,1'-biphenyl serving as a precursor for diverse organic syntheses2.

Properties

CAS Number

123640-93-7

Product Name

4,4'-Bis(triethoxysilyl)-1,1'-biphenyl

IUPAC Name

triethoxy-[4-(4-triethoxysilylphenyl)phenyl]silane

Molecular Formula

C24H38O6Si2

Molecular Weight

478.7 g/mol

InChI

InChI=1S/C24H38O6Si2/c1-7-25-31(26-8-2,27-9-3)23-17-13-21(14-18-23)22-15-19-24(20-16-22)32(28-10-4,29-11-5)30-12-6/h13-20H,7-12H2,1-6H3

InChI Key

KENDGHJJHKCUNB-UHFFFAOYSA-N

SMILES

CCO[Si](C1=CC=C(C=C1)C2=CC=C(C=C2)[Si](OCC)(OCC)OCC)(OCC)OCC

Canonical SMILES

CCO[Si](C1=CC=C(C=C1)C2=CC=C(C=C2)[Si](OCC)(OCC)OCC)(OCC)OCC

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