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CAS 1020719-26-9

:

1-(2-Chloroethoxy)-4-[1-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-2-phenyl-1-buten-1-yl-3,3,4,4,4-d<sub>5</sub>]benzene

Description:
1-(2-Chloroethoxy)-4-[1-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-2-phenyl-1-buten-1-yl-3,3,4,4,4-d5]benzene, with the CAS number 1020719-26-9, is a complex organic compound characterized by its multi-functional structure. It features a chloroethoxy group, which contributes to its reactivity and solubility in organic solvents. The presence of a dimethylsilyl group enhances its stability and may influence its interaction with other chemical species. The compound also contains multiple aromatic rings, which can provide significant π-π stacking interactions and contribute to its electronic properties. The deuterated components (indicated by the d5 notation) suggest that this compound may be used in studies requiring isotopic labeling, such as NMR spectroscopy or tracing in metabolic studies. Overall, this compound's unique structure and functional groups make it of interest in various fields, including medicinal chemistry and materials science, where it may serve as a precursor or intermediate in the synthesis of more complex molecules.
Formula:C30H37ClO2Si
InChI:InChI=1S/C30H37ClO2Si/c1-7-28(23-11-9-8-10-12-23)29(24-13-17-26(18-14-24)32-22-21-31)25-15-19-27(20-16-25)33-34(5,6)30(2,3)4/h8-20H,7,21-22H2,1-6H3/i1D3,7D2
InChI key:InChIKey=ODAPRONGKJOXCU-WRMAMSRYSA-N
SMILES:C(=C(C(C([2H])([2H])[2H])([2H])[2H])C1=CC=CC=C1)(C2=CC=C(O[Si](C(C)(C)C)(C)C)C=C2)C3=CC=C(OCCCl)C=C3
Synonyms:
  • Benzene, 1-(2-chloroethoxy)-4-[1-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-2-phenyl-1-buten-1-yl-3,3,4,4,4-d5]-
  • 1-(2-Chloroethoxy)-4-[1-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-2-phenyl-1-buten-1-yl-3,3,4,4,4-d5]benzene
  • ]benzene
  • 1-(2-Chloroethoxy)-4-[1-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-2-phenyl-1-buten-1-yl-3,3,4,4,4-d
  • (3,3,4,4,4-D5)-(E/Z)-1-[4-(2-Chloroethoxy)phenyl]-1-[4-(t-butyldimethylsilyloxy)phenyl]-2-phenyl-1-butene
  • 5
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