(Diacetoxyiodo)benzene - 98%, high purity , CAS No.3240-34-4

1 Citations
  • ≥98%
Item Number
D106797
Grouped product items
SKUSizeAvailabilityPrice Qty
D106797-5g
5g
In stock
$15.90
D106797-10g
10g
In stock
$23.90
D106797-25g
25g
In stock
$44.90
D106797-100g
100g
In stock
$160.90
D106797-500g
500g
In stock
$659.90

Basic Description

Synonyms(Diacetoxyiodo)benzene | Iodobenzene diacetate | 3240-34-4 | Iodosobenzene diacetate | Phenyliodo diacetate | Phenyliodoso acetate | Phenyliodine diacetate | Phenyliodoso diacetate | Bis(acetato)phenyliodine | Benzene, (diacetoxyiodo)- | Phenyliodine(III) diacetate | Phenyliod
Specifications & Purity≥98%
Storage TempArgon charged
Shipped InNormal
Product Description

Stoichiometric oxidant in the TEMPO oxidation of nerol to neral. Oxidant employed in the rhodium-catalyzed aziridination of olefins with sulfamate esters. Unactivated sp3 C-H bonds of both oxime and pyridine substrates undergo highly regio- and chemoselective Pd(II)-catalyzed oxygenation with PhI(OAc)2 as a stoichiometric oxidant. Used in the room temperature Pd-catalyzed 2-arylation of indoles Useful reagent for the synthesis of a wide variety of heterocyclic compounds.

Associated Targets(Human)

POLK Tbio DNA polymerase kappa (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488185320
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185320
IUPAC Name [acetyloxy(phenyl)-λ3-iodanyl] acetate
INCHI InChI=1S/C10H11IO4/c1-8(12)14-11(15-9(2)13)10-6-4-3-5-7-10/h3-7H,1-2H3
InChi Key ZBIKORITPGTTGI-UHFFFAOYSA-N
Canonical SMILES CC(=O)OI(C1=CC=CC=C1)OC(=O)C
Isomeric SMILES CC(=O)OI(C1=CC=CC=C1)OC(=O)C
WGK Germany 3
RTECS DA3525000
PubChem CID 76724
Molecular Weight 322.1
Beilstein 1879369
Reaxy-Rn 1879369

Certificates

Certificate of Analysis(COA)

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26 results found

Lot NumberCertificate TypeDateItem
L2216804Certificate of AnalysisSep 10, 2024 D106797
C2414369Certificate of AnalysisFeb 29, 2024 D106797
B2427379Certificate of AnalysisFeb 04, 2024 D106797
B2427376Certificate of AnalysisFeb 04, 2024 D106797
B2427369Certificate of AnalysisFeb 04, 2024 D106797
B2221217Certificate of AnalysisNov 17, 2023 D106797
B2221262Certificate of AnalysisNov 17, 2023 D106797
B2221224Certificate of AnalysisNov 17, 2023 D106797
G2310749Certificate of AnalysisJun 13, 2023 D106797
G2310774Certificate of AnalysisJun 13, 2023 D106797
G2310770Certificate of AnalysisJun 13, 2023 D106797
G2310760Certificate of AnalysisJun 13, 2023 D106797
G2310759Certificate of AnalysisJun 13, 2023 D106797
G2310758Certificate of AnalysisJun 13, 2023 D106797
G2310757Certificate of AnalysisJun 13, 2023 D106797
G2310755Certificate of AnalysisJun 13, 2023 D106797
G2310748Certificate of AnalysisJun 13, 2023 D106797
F2116314Certificate of AnalysisMar 14, 2023 D106797
L1820040Certificate of AnalysisAug 06, 2022 D106797
F2315965Certificate of AnalysisDec 24, 2021 D106797
E2310075Certificate of AnalysisDec 24, 2021 D106797
B2219153Certificate of AnalysisDec 24, 2021 D106797
B2307094Certificate of AnalysisApr 19, 2021 D106797
F2118117Certificate of AnalysisApr 19, 2021 D106797
F2116290Certificate of AnalysisApr 19, 2021 D106797
F2116092Certificate of AnalysisApr 19, 2021 D106797

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Chemical and Physical Properties

SolubilityInsoluble in water. Solubility in Methanol almost transparency.
Sensitivitylight sensitive; Moisture sensitive
Melt Point(°C)161-165°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H302:Harmful if swallowed

H312:Harmful in contact with skin

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P317:IF SWALLOWED: Get medical help.

P317:Get emergency medical help.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS DA3525000
Reaxy-Rn 1879369

Related Documents

Citations of This Product

1. Xiaolei Ren, Jinwu Bai, Xingxing Gu, Hui Xu, Bochuan Tan, Shenying Xu, Jiangyu Hao, Fang Gao, Xin Li.  (2022)  Insight into the anti-corrosion performance of three imidazo-pyridazines for Al alloy in different concentrations of hydrochloric acid solutions.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,  113  (348).  [PMID:]

References

1. S K Vaidya,C Damodaran.  (1982-01-01)  Determination of vitamin C in tablets and fruits by titration with phenyliodosoacetate..  Il Farmaco; edizione pratica,  37  ((1)): (9-14).  [PMID:7056375]
2. G Wells,A Seaton,M F Stevens.  (2000-04-26)  Structural studies on bioactive compounds. 32. Oxidation of tyrphostin protein tyrosine kinase inhibitors with hypervalent iodine reagents..  Journal of medicinal chemistry,  43  ((8)): (1550-1562).  [PMID:10780912]
3. K C Nicolaou,Vikrant A Adsool,Christopher R H Hale.  (2010-03-03)  An expedient procedure for the oxidative cleavage of olefinic bonds with PhI(OAc)2, NMO, and catalytic OsO4..  Organic letters,  12  ((7)): (1552-1555).  [PMID:20192259]
4. Jinbo Huang,Yimiao He,Yong Wang,Qiang Zhu.  (2012-09-22)  Synthesis of benzimidazoles by PIDA-promoted direct C(sp2)-H imidation of N-arylamidines..  Chemistry (Weinheim an der Bergstrasse, Germany),  18  ((44)): (13964-13967).  [PMID:22996950]
5. Chunying Gao,Mackenzie C Bergagnini-Kolev,Michael Z Liao,Zhican Wang,Timothy Wong,Justina C Calamia,Yvonne S Lin,Qingcheng Mao,Kenneth E Thummel.  (2017-06-18)  Simultaneous quantification of 25-hydroxyvitamin D3-3-sulfate and 25-hydroxyvitamin D3-3-glucuronide in human serum and plasma using liquid chromatography-tandem mass spectrometry coupled with DAPTAD-derivatization..  Journal of chromatography. B, Analytical technologies in the biomedical and life sciences,  1060  (158-165).  [PMID:28622619]
6. Simon Roehrer,Juergen Behr,Verena Stork,Mara Ramires,Guillaume Médard,Oliver Frank,Karin Kleigrewe,Thomas Hofmann,Mirjana Minceva.  (2018-07-28)  Xanthohumol C, a minor bioactive hop compound: Production, purification strategies and antimicrobial test..  Journal of chromatography. B, Analytical technologies in the biomedical and life sciences,  1095  (39-49).  [PMID:30053686]
7. Bikash Dangi,Hyun Park,Tae-Jin Oh.  (2018-08-24)  Effects of Alternative Redox Partners and Oxidizing Agents on CYP154C8 Catalytic Activity and Product Distribution..  Chembiochem : a European journal of chemical biology,  19  ((21)): (2273-2282).  [PMID:30136363]
8. S Garadnay,P Herczegh,S Makleit,T Friedmann,P Riba,S Fürst.  (2001-04-03)  Reactions of morphine derivatives with phenyliodo(III)diacetate (PIDA): synthesis of new morphine analogues..  Current medicinal chemistry,  ((6)): (621-626).  [PMID:11281845]
9. Lopa V Desai,Kami L Hull,Melanie S Sanford.  (2004-08-05)  Palladium-catalyzed oxygenation of unactivated sp3 C-H bonds..  Journal of the American Chemical Society,  126  ((31)): (9542-9543).  [PMID:15291549]
10. Renhua Fan,Weixun Li,Bing Wang.  (2008-11-29)  A one-pot oxidative decarboxylation-Friedel-Crafts reaction of acyclic alpha-amino acid derivatives activated by the combination of iodobenzene diacetate/iodine and iron dust..  Organic & biomolecular chemistry,  ((24)): (4615-4621).  [PMID:19039371]
11. Xiaolei Ren, Jinwu Bai, Xingxing Gu, Hui Xu, Bochuan Tan, Shenying Xu, Jiangyu Hao, Fang Gao, Xin Li.  (2022)  Insight into the anti-corrosion performance of three imidazo-pyridazines for Al alloy in different concentrations of hydrochloric acid solutions.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,  113  (348).  [PMID:]

Solution Calculators