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化驗
97%
形狀
solid
mp
109-110 °C (lit.)
官能基
aldehyde
iodo
SMILES 字串
Oc1c(I)cc(I)cc1C=O
InChI
1S/C7H4I2O2/c8-5-1-4(3-10)7(11)6(9)2-5/h1-3,11H
InChI 密鑰
MYWSBJKVOUZCIA-UHFFFAOYSA-N
相关类别
應用
3,5-Diiodosalicylaldehyde has been used in the synthesis of:
- new Schiff bases, (2,4-diiodo-6-[(2-morpholin-4-yl-ethylimino)-methyl]-phenol and 2,4-diiodo-6-[(3-morpholin-4-yl-propylimino)-methyl]-phenol)
- new tridentate ligand, [(2-hydroxy-3,5-diiodo-benzylidene)-amino]-acetic acid (HDBA)
- 3-bromo-N′-(2-hydroxy-3,5-diiodobenzylidene)benzohydrazide monohydrate
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Synthesis and antibacterial activities of copper (II) with [(2-hydroxy-3, 5-diiodo-benzylidene)-amino]-acetic acid.
Xu S-P, et al.
Journal of Coordination Chemistry, 63(19), 3463-3470 (2010)
Ganesan Jeya Shree et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 226, 117613-117613 (2019-10-14)
In this work, we designed a novel Schiff-base probe from the condensation reaction of 3,5-diiodosalicylaldehyde with isoniazid. Treatment of the sensor molecule with different metal ions like K+, Ba2+, Ca2+, Mg2+, Fe2+, Mn2+, Co2+, Cu2+, Cd2+, Ni2+, Hg2+, Zn2+, Pb2+
Synthesis and antibacterial activities of metal (II) complexes with Schiff bases derived from 3, 5-diiodosalicylaldehyde.
Xu S-P, et al.
Journal of Coordination Chemistry, 62(12), 2048-2057 (2009)
Jing-Heng Ning et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 4), o905-o906 (2009-01-01)
Crystals of the title compound, C(14)H(9)BrI(2)N(2)O(2)·H(2)O, were obtained from a condensation reaction of 3-bromo-benzohydrazide with 3,5-diiodo-salicylaldehyde. The Schiff base mol-ecule assumes an E configuration with respect to the C=N bond, and the dihedral angle between the two benzene rings is
Yang Pan et al.
Chemosphere, 144, 2312-2320 (2015-11-26)
During drinking water disinfection, iodinated disinfection byproducts (I-DBPs) can be generated through reactions between iodide, disinfectants, and natural organic matter. Drinking water I-DBPs have been increasingly attracting attention as emerging organic pollutants as a result of their significantly higher toxicity
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