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(Diacetoxyiodo)benzene

CAS No.
3240-34-4
Chemical Name:
(Diacetoxyiodo)benzene
Synonyms
PhI(OAc)2;BAIB;IODOBENZENE DIACETATE;DAIB;[Bis(acetoxy)iodo]benzene;PIA;PHENYLIODINE DIACETATE;IODOSOBENZENE DIACETATE;Phenyliodoso diacetate;IODOBENZENE I,I-DIACETATE
CBNumber:
CB2222138
Molecular Formula:
C10H11IO4
Molecular Weight:
322.1
MDL Number:
MFCD00008692
MOL File:
3240-34-4.mol
MSDS File:
SDS
Last updated:2025-09-25 19:11:34
Product description Number Pack Size Price
(Diacetoxyiodo)benzene 98% 178721 5g $26
(Diacetoxyiodo)benzene 98% 178721 25g $71.5
Monoclonal Anti-RICTOR antibody produced in mouse clone 1F3, purified immunoglobulin, buffered aqueous solution WH0253260M1 100 μg $406
Monoclonal Anti-RICTOR antibody produced in mouse clone 7B3, ascites fluid SAB5300210 100 μL $541
Iodobenzene Diacetate >97.0%(T) I0330 10g $27
More product size

(Diacetoxyiodo)benzene Properties

Melting point 161-163 °C (lit.)
Density 1.6865 (estimate)
refractive index n/D 1.444
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility INSOLUBLE
form Solution
color Clear to cloudy colorless to yellow
biological source mouse
Water Solubility INSOLUBLE
Sensitive Light Sensitive
BRN 1879369
Stability Light and Moisture sensitive
InChIKey ZBIKORITPGTTGI-UHFFFAOYSA-N
CAS DataBase Reference 3240-34-4(CAS DataBase Reference)
EWG's Food Scores 1
NIST Chemistry Reference Iodobenzene diacetate(3240-34-4)
EPA Substance Registry System Iodine, bis(acetato-.kappa.O)phenyl- (3240-34-4)
UNSPSC Code 12352203
NACRES NA.41

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-37/39-26-36/37/39-27
RIDADR  1479
WGK Germany  3
RTECS  DA3525000
4.10-8
Hazard Note  Irritant
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29310095
NFPA 704
1
2 1

(Diacetoxyiodo)benzene price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 178721 (Diacetoxyiodo)benzene 98% 3240-34-4 5g $26 2025-07-31 Buy
Sigma-Aldrich 178721 (Diacetoxyiodo)benzene 98% 3240-34-4 25g $71.5 2025-07-31 Buy
Sigma-Aldrich WH0253260M1 Monoclonal Anti-RICTOR antibody produced in mouse clone 1F3, purified immunoglobulin, buffered aqueous solution 100 μg $406 2025-07-31 Buy
Sigma-Aldrich SAB5300210 Monoclonal Anti-RICTOR antibody produced in mouse clone 7B3, ascites fluid 100 μL $541 2025-07-31 Buy
TCI Chemical I0330 Iodobenzene Diacetate >97.0%(T) 3240-34-4 10g $27 2025-07-31 Buy
Product number Packaging Price Buy
178721 5g $26 Buy
178721 25g $71.5 Buy
WH0253260M1 100 μg $406 Buy
SAB5300210 100 μL $541 Buy
I0330 10g $27 Buy

(Diacetoxyiodo)benzene Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powder

Uses

(Diacetoxyiodo)benzene is a hypervalent iodine reagent that is used in conjunction with catalytic amount of sodium azide in acetonitrile, which enables oxidative decarboxylation of 2-aryl carboxylic acid into the corresponding aldehydes, ketones and nitriles.

Application

(Diacetoxyiodo)benzene, an oxidizing agent, has a wide range of applications. (Diacetoxyiodo)benzene, also known as Diacetoxy Iodobenzene, is used in wide range of medicals industrial applications as well as in human and animal nutrition products such as antiseptics and disinfectants, pharmaceutical intermediates, polarizing films for liquid crystal display [LCD] chemicals.

Origin

This reagent was originally prepared by Conrad Willgerod by reacting iodobenzene with a mixture of acetic acid and peracetic acid: 
C6H5I + CH3CO3H + CH3CO2H → C6H5I(O2CCH3)2 + H2O

reaction suitability

reagent type: catalyst
reagent type: oxidant
reaction type: C-H Activation

Biological Activity

RPTOR independent companion of MTOR complex 2 (RICTOR) maintains stability of the mechanistic target of rapamycin (mTOR) complex 2. It also has a role in neutrophil chemotaxis and has been linked to prostate cancer.

Synthesis

Iodobenzene

591-50-4

Acetaldehyde

75-07-0

(Diacetoxyiodo)benzene

3240-34-4

GENERAL STEPS: In a typical experiment, glacial acetic acid (2 mL), iodobenzene (0.401 mmol), and cobalt chloride hexahydrate (0.004 mmol, 1 mol%) were added to a 20 mL scintillation vial and a rubber septum was assembled. The reaction vessel was purged with oxygen for 5 min, and then acetaldehyde (4.07 mmol, 10.2 eq.) was added all at once. The reaction mixture was stirred at 1 atmosphere of oxygen and reacted at 23°C for 5 h via an inflated balloon. After completion of the reaction, the solvent was removed under vacuum and the residue was dissolved in dichloromethane. The organic layer was washed with distilled water and extracted with dichloromethane (3 x 7 mL). The organic layers were combined, dried with anhydrous magnesium sulfate and the solvent was removed in vacuum to give iodobenzene diacetic acid. The isolated compounds were characterized by 1H NMR and 13C NMR spectroscopy.

Purification Methods

The purity of diacetoxyiodobenzene can be checked by treatment with H2SO4 then KI and the liberated I2 is estimated with standard thiosulfate. It has been recrystallised from 5M acetic acid and dried overnight in a vacuum desiccator over CaCl2. The surface of the crystals may become slightly yellow but this does not affect its usefulness. [Sharefkin & Saltzman Org Synth Coll Vol V 600 1973, Beilstein 5 IV 693.]

References

[1] Nature Chemistry, 2018, vol. 10, # 2, p. 200 - 204

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View Lastest Price from (Diacetoxyiodo)benzene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(Diacetoxyiodo)benzene pictures 2025-10-14 (Diacetoxyiodo)benzene
3240-34-4
0.99 RongNa Biotechnology Co.,Ltd
Iodobenzene diacetate pictures 2025-10-14 Iodobenzene diacetate
3240-34-4
US $50.00-80.00 / kg 100kg 99% 200mt Jinan Finer Chemical Co., Ltd
(Diacetoxyiodo)benzene pictures 2025-10-11 (Diacetoxyiodo)benzene
3240-34-4
US $10.00 / KG 1KG 99% 100 mt Hebei Chuanghai Biotechnology Co., Ltd
PHENYLIODINE DIACETATE PIA AURORA KA-6690 (DIACETOXYIODO)BENZENE DIACETOXYIODOSOBENZENE DAIB LABOTEST-BB LT00847235 IODOBENZENE I,I-DIACETATE IODOBENZENE DIACETATE IODOSOBENZENE DIACETATE IODOSOBENZENE I,I-DIACETATE IODINE, BIS(ACETATO-KO)PHENYL (Diacetoxyiodo)benzene PIDA IODOSOBENZENE DIACETATE FOR SYNTHESIS (Diacetoxyiodo)benze (Diacetoxyiodo)benzene~DIB~Iodobenzene diacetate~Phenyliodine(III) diacetate iodosylbenzene di(acetate) BAIB 2-[2-(carboxylatoMethyl)-3-iodophenyl]acetate Lodobenzene diacetate Iodobenzene diacetate, 98% 100GR Iodobenzene diacetate, 98% 25GR (diacetoxyiodo)-benzen (dihydroxyiodo)-benzendiacetate Benzene, (diacetoxyiodo)- Benzene, iodoso-, diacetate Bis(acetato)phenyliodine bis(acetato-o)phenyl-iodin Iodine, bis(acetato-O)phenyl- iodoso-benzendiacetate phenyliodine(iii)diacetate Phenyliodo diacetate phenyliododiacetate Phenyliodoso acetate Phenyliodoso diacetate phenyliodosodiacetate phenyliodosyldiacetate Iodobenzene 1,1-diacetate acetic acid coMpound with iodosylbenzene (2:1) (Diacetoxyiodo)benzene, Bis(acetoxy)(phenyl)iodane Iodosobenzene diacetate ,PIDA Theiodoethyl ester two acetic acid coMpound with iodobenzene (2:1) DKFZp686B11164 KIAA1999 mAVO3 MGC39830 Monoclonal Anti-RICTOR antibody produced in mouse PhI(OAc)2 [acetyloxy(phenyl)-λ3-iodanyl] acetate [acetyloxy(phenyl)-$l^{3}-iodanyl] acetate bis(acetyloxy)(phenyl)-lambda~ (Diacetoxyiodo)benzene≥ 99% (HPLC) [acetyloxy(phenyl)-λ3-iodanyl] acetate -iodanyl acetate bis(acetato-O)phenyliodine Ethyl 2-(4-formylphenyl)2-methylpropionatephenyliodine diacetate (Diacetoxyiodo)benzene=Phenyliodosodiacetate