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Merck
CN

263826

Sigma-Aldrich

4-碘苯甲醛

96%

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About This Item

线性分子式:
IC6H4CHO
CAS号:
分子量:
232.02
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

96%

mp

78-82 °C (lit.)

官能团

aldehyde
iodo

储存温度

2-8°C

SMILES字符串

Ic1ccc(C=O)cc1

InChI

1S/C7H5IO/c8-7-3-1-6(5-9)2-4-7/h1-5H

InChI key

NIEBHDXUIJSHSL-UHFFFAOYSA-N

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一般描述

4-碘苯甲醛参与Suzuki–Miyaura偶联反应产生金属–有机骨架催化剂。

应用

4-碘苯醛用于制备:
  • 苄叉二胺单层
  • 4-[2-(三甲基硅基)乙炔基] 苯甲醛
  • 5,15-二均三苯-10-(3-[2-(三甲基硅基)乙炔基] 苯基 }-20-(4-碘苯基)卟啉
  • 5,15-二甲基异亚丙基-10-[3,5- {2-[4-( N,N ′-二氟硼基-1,9-二甲基吡喃-5-基)-苯基 ] 乙炔基 } 苯基 ]-20-(4-碘苯基)卟啉,多色素构建块

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Trans-Substituted porphyrin building blocks bearing iodo and ethynyl groups for applications in bioorganic and materials chemistry.
Ravikanth M, et al.
Tetrahedron, 54(27), 7721-7734 (1998)
Selective cleavage of the carbon-halide bond in substituted benzaldimine monolayers by synchrotron soft X-ray: Anomalously large cleavage rate of the carbon-bromide bond.
Moon JH, et al.
Langmuir, 16(6), 2981-2984 (2000)
Amino-Induced 2D Cu-Based Metal--Organic Framework as an Efficient Heterogeneous Catalyst for Aerobic Oxidation of Olefins
Tang J, et al.
Chemistry?A European Journal , 26, 4333-4340 (2020)
Umar Ali Dar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 240, 118570-118570 (2020-06-27)
The current study determines optical and fluorescence response of halogen substituted series of meso‑tetrakis‑(4‑halophenyl) porphyrin; H2TXPP (Halo = F, Cl, Br, I) dye in tetrahydrofuran; THF and THF-water system at changing pH in relationship with changing medium of allure. Effects produced
Abel T Demissie et al.
Journal of the American Chemical Society, 137(27), 8819-8828 (2015-06-23)
We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a self-assembled monolayer (SAM) of 4-formylthiophenol or 4-aminothiophenol on Au, followed by repetitive, alternate addition of terephthalaldehyde

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