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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
2-Iodobenzaldehyde, 97%
InChI
1S/C7H5IO/c8-7-4-2-1-3-6(7)5-9/h1-5H
SMILES string
Ic1ccccc1C=O
InChI key
WWKKTHALZAYYAI-UHFFFAOYSA-N
assay
97%
mp
36-39 °C (lit.)
functional group
aldehyde
iodo
storage temp.
2-8°C
Quality Level
Related Categories
Application
2-Iodobenzaldehyde may be used as a reactant in the synthesis of the following heterocycles:
- 2,3-diaryl-1-indenones
- indolo[1,2-a]quinazolines
- Baylis-Hillman (BH) adducts
- 5-phenylindazolo[3,2-b]quinazolin-7(5H)-one
- 4-(3-iodophenyl)-2,2:6,2-terpyridine
- fluoren-9-one
- 2-formyl-3′-methoxybiphenyl
General description
2-Iodobenzaldehyde (o-iodobenzaldehyde) is a 2-halobenzaldehyde derivative. Its crystals belong to the orthorhombic crystal system and P212121 space group.
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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Self-Assembly of Shape-Persistent Hexagonal Macrocycles with Trimeric Bis (terpyridine)-FeII Connectivity.
Li S, et al.
European Journal of Organic Chemistry, 2008(19), 3328-3334 (2008)
Synthesis of indanones via intramolecular Heck reaction of Baylis-Hillman adducts of 2-iodobenzaldehyde.
Park JB, et al.
Bull. Korean Chem. Soc., 25(6), 927-930 (2004)
Combined catalysis: Pd-catalyzed two-step one-pot protocol for 2, 3-diaryl-1-indenones involving domino synthesis of diarylacetylenes and Heck-Larock annulations.
Rao MLN and Dhanorkar RJ.
Tetrahedron, 70(43), 8067-8078 (2014)
2-Iodobenzaldehyde.
Betz R and Klufers P.
Acta Crystallographica Section E, Structure Reports Online, 63(12), o4879-o4879 (2007)
Ring-Closing Olefin Metathesis of 2, 2'-Divinylbiphenyls: A Novel and General Approach to Phenanthrenes.
Iuliano A, et al.
Organic Letters, 6(21), 3711-3714 (2004)
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