Home Iodos 629-09-4
629-09-4,MFCD00001103
Catalog No.:AA003DOH

629-09-4 | 1,6-Diiodohexane

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5g
98% (stabilized with Copper chip)
in stock  
$8.00   $6.00
- +
25g
98% (stabilized with Copper chip)
in stock  
$38.00   $27.00
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100g
98% (stabilized with Copper chip)
in stock  
$131.00   $92.00
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500g
98% (stabilized with Copper chip)
in stock  
$513.00   $359.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003DOH
Chemical Name:
1,6-Diiodohexane
CAS Number:
629-09-4
Molecular Formula:
C6H12I2
Molecular Weight:
337.9684
MDL Number:
MFCD00001103
SMILES:
ICCCCCCI
Properties
Properties
 
BP:
141-142 °C (10 mmHg)  
Form:
Liquid  
MP:
9-10 °C  
Refractive Index:
1.5852-1.5872  
Stability:
Light Sensitive  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
31.5  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Rotatable Bond Count:
5  
XLogP3:
4.6  

Upstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2018,vol.57,#36,p.11564-11568

[2]Angew.Chem.,2018,vol.130,#36,p.11738-11742,5

[3]JournalfuerPraktischeChemie(Leipzig),1960,vol.10,p.265-289

[4]JournalofChemicalResearch,Miniprint,1983,#1,p.101-132

[5]Patent:US5272167,1993,A,

[6]Patent:US4851423,1989,A,

[1]Heterocycles,1986,vol.24,#11,p.3043-3046

[1]Tetrahedron,2005,vol.61,#23,p.5529-5534

[1]ChemischeBerichte,1928,vol.61,p.570

[2]OrganicSyntheses,1951,vol.31,p.32

[1]Steroids,1983,vol.41,#3,p.285-290

Downstream Synthesis Route

[1]JournalofPharmacyandPharmacology,1959,vol.11,p.80,86

[2]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.3067-3071

[3]Patent:WO2005/66129,2005,A2.Locationinpatent:Page/Pagecolumn19

[1]SupramolecularChemistry,2014,vol.26,p.182-191

[2]JournaloftheChemicalSociety,1958,p.1489,1497

[3]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.3067-3071

[4]Patent:WO2005/66129,2005,A2.Locationinpatent:Page/Pagecolumn28

[1]JournalofPharmacyandPharmacology,1959,vol.11,p.80,86

[1]BioorganicandMedicinalChemistry,2015,vol.23,p.5954-5971

[2]Patent:WO2016/176343,2016,A1.Locationinpatent:Paragraph00339

[3]AnnalesdeChimie(Cachan,France),1915,vol.<9>3,p.201,220    BulletindelaSocieteChimiquedeFrance,1910,vol.<4>7,p.329

[1]JournaloftheChemicalSociety,1958,p.1489,1497

[2]Patent:WO2015/116707,2015,A1.Locationinpatent:Paragraph1175

[3]Patent:WO2017/19822,2017,A1.Locationinpatent:Paragraph974;988

[4]Patent:WO2017/19817,2017,A1.Locationinpatent:Paragraph951

[5]Patent:WO2017/19830,2017,A1.Locationinpatent:Paragraph949;950;963;934

[6]Patent:WO2017/19832,2017,A1.Locationinpatent:Paragraph1203

[7]Patent:WO2017/19833,2017,A1.Locationinpatent:Paragraph1188;1202

[8]Patent:WO2019/222272,2019,A1.Locationinpatent:Page/Pagecolumn254;255

Literature

Title: Tissue plasminogen activator-containing polyurethane surfaces for fibrinolytic activity.

Journal: Acta biomaterialia 20110501

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SDS
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