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1-n-Butyl-4-iodobenzene, 98%, Thermo Scientific Chemicals
化学物質識別子
CAS20651-67-6
IUPAC Name1-butyl-4-iodobenzene
Molecular FormulaC10H13I
InChI KeyXILRUONFYBUYIE-UHFFFAOYSA-N
SMILESCCCCC1=CC=C(I)C=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to yellow
Assay (GC)≥97.5%
FormLiquid
Refractive Index1.5665-1.5705 @ 20?C
It is used as an active pharmaceutical intermediate. It is also used in the synthesis and characterization of photoelectronic polymers containing triphenylamine moiety and in the palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is used as an active pharmaceutical intermediate. It is also used in the synthesis and characterization of photoelectronic polymers containing triphenylamine moiety and in the palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.
Solubility
Sparingly soluble in water at 25°C 3.6E-3 g/L.
Notes
Light sensitive. Store away from light and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
It is used as an active pharmaceutical intermediate. It is also used in the synthesis and characterization of photoelectronic polymers containing triphenylamine moiety and in the palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.
Solubility
Sparingly soluble in water at 25°C 3.6E-3 g/L.
Notes
Light sensitive. Store away from light and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Yingliang Liua, et al. Synthesis and characterization of photoelectronic polymers containing triphenylamine moiety.React. Funct. Polym.,2007,67(3), 253-263.
- Pan, et al. Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to Bromides and Chlorides.J Am Chem Soc., Org. Lett.,2010,132(40), 14076-14078.