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Safety Information

252115

Sigma-Aldrich

2-Iodobenzoyl chloride

98%

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About This Item

Linear Formula:
IC6H4COCl
CAS Number:
Molecular Weight:
266.46
Beilstein:
2042672
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

bp

105-106 °C/1 mmHg (lit.)

mp

27-31 °C (lit.)

functional group

acyl chloride
iodo

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

252115-BULK:
252115-5G:4548173987378
252115-VAR:
252115-25G:


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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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