Skip to Content
Merck
All Photos(2)

Documents

252115

Sigma-Aldrich

2-Iodobenzoyl chloride

98%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
IC6H4COCl
CAS Number:
609-67-6
Molecular Weight:
266.46
Beilstein:
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

Looking for similar products? Visit Product Comparison Guide

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

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

N-Methylaniline 98%

Sigma-Aldrich

M29304

N-Methylaniline

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service