Home Iodos 615-42-9
615-42-9,MFCD00001038
Catalog No.:AA00E8LK

615-42-9 | 1,2-Diiodobenzene

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1g
98% (stabilized with Copper chip)
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$6.00   $4.00
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5g
98% (stabilized with Copper chip)
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$12.00   $8.00
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10g
98% (stabilized with Copper chip)
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$17.00   $12.00
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25g
98% (stabilized with Copper chip)
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$22.00   $15.00
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100g
98% (stabilized with Copper chip)
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$61.00   $43.00
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500g
98% (stabilized with Copper chip)
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$284.00   $199.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00E8LK
Chemical Name:
1,2-Diiodobenzene
CAS Number:
615-42-9
Molecular Formula:
C6H4I2
Molecular Weight:
329.9049
MDL Number:
MFCD00001038
SMILES:
Ic1ccccc1I
NSC Number:
29029
Properties
Properties
 
BP:
287.0°C  
Form:
Liquid  
MP:
>300°C  
Refractive Index:
n20/D 1.718(lit.)  
Stability:
Light Sensitive  
Storage:
Light sensitive;Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
62.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
XLogP3:
3.2  

Downstream Synthesis Route

[1]JournalofOrganicChemistryUSSR(EnglishTranslation),1988,vol.24,p.2029-2035    ZhurnalOrganicheskoiKhimii,1988,vol.24,p.2251-2258

[2]JournalofOrganicChemistryUSSR(EnglishTranslation),1988,vol.24,p.2029-2035    ZhurnalOrganicheskoiKhimii,1988,vol.24,p.2251-2258

[1]Wójcik,Przemysław;Trzeciak,AnnaM.[AppliedCatalysisA:General,2018,vol.560,p.73-83]

[2]Khedkar,MayurV.;Khan,ShoebR.;Sawant,DineshN.;Bagal,DattatrayaB.;Bhanage,BhalchandraM.[AdvancedSynthesisandCatalysis,2011,vol.353,#18,p.3415-3422]

[3]Perry,RobertJ.;Turner,S.Richard[JournalofOrganicChemistry,1991,vol.56,#23,p.6573-6579]

[1]Wójcik,Przemysław;Trzeciak,AnnaM.[AppliedCatalysisA:General,2018,vol.560,p.73-83]

[2]Perry,RobertJ.;Turner,S.Richard[JournalofOrganicChemistry,1991,vol.56,#23,p.6573-6579]

[1]Khedkar,MayurV.;Khan,ShoebR.;Sawant,DineshN.;Bagal,DattatrayaB.;Bhanage,BhalchandraM.[AdvancedSynthesisandCatalysis,2011,vol.353,#18,p.3415-3422]

[2]Perry,RobertJ.;Turner,S.Richard[JournalofOrganicChemistry,1991,vol.56,#23,p.6573-6579]

[3]Wójcik,Przemysław;Trzeciak,AnnaM.[AppliedCatalysisA:General,2018,vol.560,p.73-83]

[1]AdvancedSynthesisandCatalysis,2011,vol.353,p.3415-3422

[2]AppliedCatalysisA:General,2018,vol.560,p.73-83

[3]JournalofOrganicChemistry,1991,vol.56,p.6573-6579

[4]AdvancedSynthesisandCatalysis,2016,vol.358,p.314-320

Literature

Title: Remarkably selective recognition of iodobenzene derivatives by a macrocyclic bis-Pt(II) metallohost.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20111216

Title: Intramolecular direct C-H arylation approach to fused purines. Synthesis of purino[8,9-f]phenanthridines and 5,6-dihydropurino[8,9-a]isoquinolines.

Journal: The Journal of organic chemistry 20100402

Title: A preliminary assessment of the effects of ATI-2042 in subjects with paroxysmal atrial fibrillation using implanted pacemaker methodology.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 20090401

Title: 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.

Journal: Organic & biomolecular chemistry 20081221

Title: Highly luminescent BODIPY-based organoboron polymer exhibiting supramolecular self-assemble structure.

Journal: Journal of the American Chemical Society 20081119

Title: A versatile route to 3-benzoheteroepines containing group 15 and 16 heavier elements involving several novel ring systems, and their thermal stabilities.

Journal: Chemical & pharmaceutical bulletin 20031101

Title: Heterolytic activation of hydrogen as a trigger for iridium complex promoted activation of carbon-fluorine bonds.

Journal: Inorganic chemistry 20020422

Title: Cationic complexes of iridium: diiodobenzene chelation, electrophilic behavior with olefins, and fluxionality of an Ir(I) ethylene complex.

Journal: Inorganic chemistry 20020422

Title: Laurenanes: fenestranes with a twist.

Journal: The Journal of organic chemistry 20010921

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