2-Iodoxybenzoic acid

CAS: 61717-82-6 Appearance: White to cream colored crystals Purity: ≥99% Capacity: 200mt/year MOQ: 220g Application: Organic Intermediate Standard: Enterprise export Manufacturer: Jinan Finer Chemi...

Introduction

CAS: 61717-82-6

Appearance: White to cream colored crystals

Purity: ≥99%

Capacity: 200mt/year

MOQ: 220g

Application: Organic Intermediate

Standard: Enterprise export

Manufacturer: Jinan Finer Chemical Co., Ltd

Synonyms: 1-Hydroxy-1.3-dioxo-3H-benz[d][1.2]iodoxol

1-Hydroxy-3H-benz[d][1.2]iodoxol-1.3-dione

Molecular Formula: C7H5IO4

Molecular Weight: 280.02

CAS Registry Number: 61717-82-6

Melting point: 280 ºC

Names and Identifiers

Name 2-Iodoxybenzoic acid
Synonyms IBX
Iodoxybenzoic aci
2-iodylbenzoic acid
2-Iodoxybenzoic acid
2-(iodooxy)benzoic acid
2-Iodoxybenzoic Acid Stabilized (SIBX)
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
1-hydroxy-1lambda~3~,2-benziodoxol-3(1H)-one 1-oxide
SIBX, 1,3-Dihydro-1,3-dioxo-1-hydroxy-1,2-benziodoxole stabilised
2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid)
CAS 61717-82-6
EINECS 629-407-7
InChI InChI=1/C7H5IO3/c8-11-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
InChIKey CQMJEZQEVXQEJB-UHFFFAOYSA-N

​Physico-chemical Properties

Molecular Formula C7H5IO4
Molar Mass 280.02
Density 2.058g/cm3
Melting Point 280 °C
Boling Point 331.824°C at 760 mmHg
Flash Point 154.482°C
Vapor Presure 0mmHg at 25°C
Appearance Solid
Color White to Almost white
Merck 14,5048
Storage Condition under inert gas (nitrogen or Argon) at 2–8 °C
Refractive Index 1.675
MDL MFCD02912492

Risk and Safety

Risk Codes R22 – Harmful if swallowed
R34 – Causes burns
R44 – Risk of explosion if heated under confinement
R42/43 – May cause sensitization by inhalation and skin contact.
R36/37/38 – Irritating to eyes, respiratory system and skin.
R20/21/22 – Harmful by inhalation, in contact with skin and if swallowed.
R37 – Irritating to the respiratory system
R35 – Causes severe burns
R1 – Explosive when dry
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
S45 – In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S22 – Do not breathe dust.
S35 – This material and its container must be disposed of in a safe way.
UN IDs UN 1759 8/PG 2
WGK Germany 3
HS Code 29163990
Hazard Class 8
Packing Group

Reference Information

Use 2-iodoylbenzoic acid is used for the oxidation of alcohols in organic synthesis. It is also often used for the preparation of Dess-Martin high iodine.
important oxidant
Overview in the past 20 years, hypervalent iodine reagents as oxidants, because of its mild reaction conditions, high yields, the characteristics of good selectivity and environmental friendliness have attracted more and more attention of chemists. 1,1, 1-triethoxyyl-1, 1-dihydroxy-1, 2-benzoiodo-3 (1H)-One (DMP,Dess-Martin periodinane) it is a typical iodine reagent, which has been widely used in organic synthesis. DMP is obtained by heating a mixed solution of 2-iodoylbenzoic acid (IBX) with acetic acid and acetic anhydride. IBX was synthesized in 1893 and has a history of 112 years. However, due to its low solubility in most common organic solvents, there are few reports on its application. In 1994, Frigerio found that IBX was soluble in DMSO, and it was used to oxidize alcohols and 1,2-ortho-diol very well, thus opening a new chapter in the application of IBX in organic synthesis.
Main properties as an oxidant, the oxidation of primary and secondary alcohols in DMSO exhibits properties similar to those of DMP, when the alcohol has a multifunctional group, IBX has better selectivity than DMP; In addition, DMP is unstable and cannot be stored for a long time, and must be prepared before use, which is inconvenient to use.
Application IBX is an inexpensive, mild oxidant, easy to prepare, and has better selectivity than DMP, can also be used for the preparation of lipid and protein metabolism improving agent oxygen male and so on. The oxidation of alcohols by IBX is usually carried out in DMSO or DMSO/THF solution, simply heating (80 °c) the alcohol, IBX and organic solvents such as ethyl acetate, chloroform, benzene, the mixture of acetonitrile, acetone, dichloromethane and the like can oxidize the primary alcohol and the secondary alcohol to the corresponding aldehyde and ketone. After the reaction is finished, the insoluble by-products and solvents can be removed by filtration to obtain the corresponding carbonyl compound.

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