550760
3-Iodobenzaldehyde
97%
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About This Item
Linear Formula:
IC6H4CHO
CAS Number:
Molecular Weight:
232.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
3-Iodobenzaldehyde, 97%
InChI
1S/C7H5IO/c8-7-3-1-2-6(4-7)5-9/h1-5H
SMILES string
Ic1cccc(C=O)c1
InChI key
RZODAQZAFOBFLS-UHFFFAOYSA-N
assay
97%
mp
57-60 °C (lit.)
functional group
aldehyde
iodo
storage temp.
2-8°C
Application
3-Iodobenzaldehyde may be used as a starting material in the preparation of:
- 3-iodocinnamic acid
- 3-(3-hydroxy-3-methylbut-1-yn-1-yl)benzaldehyde
- 1,3-dihydroxy-2-(3-iodophenyl)-4,4,5,5-tetramethylimidazolidine
General description
3-Iodobenzaldehyde can be prepared by the iodination of benzaldehyde using 1,3-diiodo-5,5-dimethylhydantoin in sulfuric acid.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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1, 3-Diiodo-5,5-dimethylhydantoin-An efficient reagent for iodination of aromatic compounds.
Chaikovskii VK, et al.
Russ. J. Org. Chem., 43(9), 1291-1296 (2007)
Suzuki Reactions with Stable Organic Radicals-Synthesis of Biphenyls Substituted with Nitronyl-Nitroxide Radicals.
Stroh C, et al.
European Journal of Organic Chemistry, 2005(17), 3697-3703 (2005)
Cross-coupling of aryl iodides with paramagnetic terminal acetylenes derived from 4, 4, 5, 5-tetramethyl-2-imidazoline-1-oxyl 3-oxide.
Klyatskaya SV, et al.
Russian Chemical Bulletin, 51(1), 128-134 (2002)
Synthesis and evaluation of potent and selective human V1a receptor antagonists as potential ligands for PET or SPECT imaging.
Fabio K, et al.
Bioorganic & Medicinal Chemistry, 20(3), 1337-1345 (2012)
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