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252115

Sigma-Aldrich

2-Iodobenzoyl chloride

98%

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About This Item

Linear Formula:
IC6H4COCl
CAS Number:
609-67-6
Molecular Weight:
266.46
Beilstein/REAXYS Number:
2042672
EC Number:
210-196-1
MDL number:
MFCD00001040
UNSPSC Code:
12352100
PubChem Substance ID:
24855183
NACRES:
NA.22

assay

98%

form

solid

bp

105-106 °C/1 mmHg (lit.)

mp

27-31 °C (lit.)

SMILES string

ClC(=O)c1ccccc1I

InChI

1S/C7H4ClIO/c8-7(10)5-3-1-2-4-6(5)9/h1-4H

InChI key

MVIVDSWUOGNODP-UHFFFAOYSA-N

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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

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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