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

Synonym

Product Category

Product Code

CAS Number

MDL Number

Pubchem SID

Reaxys RN

1-chloro-1λ^{3},2-benziodoxol-3-one,NSC 191950

Non-Fluorochemicals

KUMI0F04

59457-26-0

329765696

141400

image-155171-Trimethyl(trifluoromethyl)silane_reagent.png

Specification
Applications
Safety & Regulations
Product Documents

Chemical Name

Molecular Formula

Molecular Weight

Assay

Appearance

melting Point

Packaging

Storage

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

C₇H₄ClIO₂

282.46

≥98.0%(HPLC)

White to Light yellow Powder

167-170ºC

5g,10g,20g,50g,100g and 500g

Store at room temperature

1-Chloro-1,2-benziodoxol-3(1H)-one is used for hypervalent iodine reagent for oxidation reactions. It also is employed as precursor for synthesis of the hypervalent iodine-CF₃ reagent(Togni II) for eletrophilic trifluoromethylation.

Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles. [1]

One-Pot Synthesis of Hypervalent Iodine Reagents for Electrophilic Trifluoromethylation. [2]

References:

[1] V.N.Nemykin, A.V.Maskaev, M.R.Geraskina,M.S.Yusubov, U.V.Zhdankin, Inorg. Chem., 2011, 50(12), pp 11263-11272.

[2] V.Matousek, E.Pietrasiak, R.Schwenk, A.Togni, J. Org. Chem., 2013, 78(3), pp 6763-6768.

Signal Word

Hazard Statements

Precautionary Statements

HS Code

RIDADR

Legal Information

Warning

H315,H319,H335

P280,P305+P351+P338,P337+P313

NONH for all modes of transport

1. Product Specification

2. Safety Data Sheet

Please inquire for pricing and availability of this product by writing email to sales@kumidas.com.

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

1-chloro-1λ^{3},2-benziodoxol-3-one,NSC 191950

Non-Fluorochemicals

KUMI0F04

59457-26-0

329765696

141400

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

1-Chloro-1,2-benziodoxol-3(1H)-one is used for hypervalent iodine reagent for oxidation reactions. It also is employed as precursor for synthesis of the hypervalent iodine-CF3 reagent(Togni II) for eletrophilic trifluoromethylation.

Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles. [1]

One-Pot Synthesis of Hypervalent Iodine Reagents for Electrophilic Trifluoromethylation. [2]

1-Chloro-1,2-benziodoxol-3(1H)-one is used for hypervalent iodine reagent for oxidation reactions. It also is employed as precursor for synthesis of the hypervalent iodine-CF₃ reagent(Togni II) for eletrophilic trifluoromethylation.