Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

744514

Sigma-Aldrich

1-Chloro-1,2-benziodoxol-3(1H)-one

98.0-102.0% (AT)

Synonym(s):

NSC 191950

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C7H4ClIO2
CAS Number:
59457-26-0
Molecular Weight:
282.46
Beilstein:
141400
UNSPSC Code:
12352005
PubChem Substance ID:
329765696
NACRES:
NA.22

Quality Level

100

Assay

98.0-102.0% (AT)

form

powder

functional group

iodo

storage temp.

2-8°C

SMILES string

ClI1OC(C2=CC=CC=C21)=O

InChI

1S/C7H4ClIO2/c8-9-6-4-2-1-3-5(6)7(10)11-9/h1-4H

InChI key

XSZMFYQLHGJKKD-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD8701
BCCB2684
BCBX0082
BCBN6672V
BCBN6672

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Synthesis and reaction of substituted arylalkoxyiodinanes: formation of stable bromoarylalkoxy and aryldialkoxy heterocyclic derivatives of tricoordinate organoiodine(III).
Amey, R. L. and Martin, J. C.
The Journal of Organic Chemistry, 44 (11), 1779-1784 (1979)

Articles

Fluoroalkylation: Expansion of Togni Reagents

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

Fluoroalkylation: Expansion of Togni Reagents

The fluoroalkylation toolbox now includes Togni reagents, hypervalent iodine perfluoroalkylation reagents, fluoroalkyl bromides, silanes, carboxylates, and sulfonyl fluorides for late stage fluoroalkylation.

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