252115
2-Iodobenzoyl chloride
98%
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About This Item
Linear Formula:
IC6H4COCl
CAS Number:
Molecular Weight:
266.46
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-196-1
Beilstein/REAXYS Number:
2042672
MDL number:
Assay:
98%
Form:
solid
InChI key
MVIVDSWUOGNODP-UHFFFAOYSA-N
InChI
1S/C7H4ClIO/c8-7(10)5-3-1-2-4-6(5)9/h1-4H
SMILES string
ClC(=O)c1ccccc1I
assay
98%
form
solid
bp
105-106 °C/1 mmHg (lit.)
mp
27-31 °C (lit.)
functional group
acyl chloride, iodo
Quality Level
Related Categories
Application
2-Iodobenzoyl chloride has been used in:
- palladium-catalyzed synthesis of carbomethoxy functional group-induced isoindolin-1-ones
- preparation of starting materials required for the synthesis of novel cyclic derivatives of pentavalent iodine, benziodazole oxides
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Synthesis of isoindolin-1-ones via palladium-catalyzed intermolecular coupling and heteroannulation between 2-iodobenzoyl chloride and imines.
Cho CS, et al.
Tetrahedron Letters, 41(20), 3891-3893 (2000)
Synthesis and reactions of amino acid-derived benziodazole oxides: new chiral oxidizing reagents.
Zhdankin VV, et al.
Tetrahedron Letters, 41(28), 5299-5302 (2000)
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