4-Iodobenzaldehyde, 98+%
4-Iodobenzaldehyde, 98+%
4-Iodobenzaldehyde, 98+%
Thermo Scientific Chemicals

4-Iodobenzaldehyde, 98+%

CAS: 15164-44-0 | C7H5IO | 232.02 g/mol
数量:
250 mg
1 g
5 g
製品番号(カタログ番号) L17448.03
または、製品番号L17448-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS15164-44-0
IUPAC Name4-iodobenzaldehyde
Molecular FormulaC7H5IO
InChI KeyNIEBHDXUIJSHSL-UHFFFAOYSA-N
SMILESIC1=CC=C(C=O)C=C1
さらに表示
FormCrystals or powder or crystalline powder or fused solid
Appearance (Color)White to cream to yellow to brown
Assay (GC)≥98.0%
Free acid (titration)≤1%
4-Iodobenzaldehyde is used in synthesis of 4-[2-(trimethylsilyl)ethynyl]benzaldehyde, 5,15-dimesityl-10-(3-[2-(trimethylsilyl)ethynyi]phenyl}-20-(4-iodophenyl)porphyrin, and 5,15-dimesityl-10-[3,5-bis{2-[4-(N,N?-difluoroboryl-1,9-dimethyidipyrrin-5-yl)-phenyl]ethynyl}phenyl]-20-(4-iodophenyl)porphyrin.

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
4-Iodobenzaldehyde is used in synthesis of 4-[2-(trimethylsilyl)ethynyl]benzaldehyde, 5,15-dimesityl-10-(3-[2-(trimethylsilyl)ethynyi]phenyl}-20-(4-iodophenyl)porphyrin, and 5,15-dimesityl-10-[3,5-bis{2-[4-(N,N′-difluoroboryl-1,9-dimethyidipyrrin-5-yl)-phenyl]ethynyl}phenyl]-20-(4-iodophenyl)porphyrin.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is sensitive to air and light. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Olivier Mongin.; Laurent Porrès.; Laurent Moreaux.; Jerome Mertz.; Mireille Blanchard-Desce. Synthesis and Photophysical Properties of New Conjugated Fluorophores Designed for Two-Photon-Excited Fluorescence. Org. Lett. 2002, 4 (5), 719-722.
  2. K.J.L. Paciorek.; S.R. Masuda.; J.G. Shih.; J.H. Nakahara. The synthesis of perfluoroalkyl and perfluoroalkylether substituted benzils. Journal of Fluorine Chemistry. 1991, 53 (2), 233-248.