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Home Iodos 26059-40-5
26059-40-5,MFCD11656774
Catalog No.:AA002RH1

26059-40-5 | 2-(2-Iodophenyl)ethan-1-ol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$32.00   $22.00
- +
5g
95%
in stock  
$479.00   $335.00
- +
  • 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:
AA002RH1
Chemical Name:
2-(2-Iodophenyl)ethan-1-ol
CAS Number:
26059-40-5
Molecular Formula:
C8H9IO
Molecular Weight:
248.0609
MDL Number:
MFCD11656774
SMILES:
OCCc1ccccc1I
Properties
Computed Properties
 
Complexity:
95.3  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.1  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1969,vol.91,p.6464-6470

[1]JournalofOrganicChemistry,2002,vol.67,#26,p.9428-9438

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1969,vol.91,p.6464-6470

[1]JournaloftheAmericanChemicalSociety,2014,vol.136,p.5821-5823

[2]JournalofOrganicChemistry,1996,vol.61,p.7147-7155

[3]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.6858-6862

[4]AngewandteChemie-InternationalEdition,2014,vol.53,p.3854-3858    Angew.Chem.,2014,vol.126,p.3934-3939,5

[5]AdvancedSynthesisandCatalysis,2017,vol.359,p.2345-2351

[6]EuropeanJournalofOrganicChemistry,2011,p.3178-3183

[7]OrganicLetters,2008,vol.10,p.2721-2724

[8]Journaloflabelledcompoundsandradiopharmaceuticals,2004,vol.47,p.591-598

[9]AngewandteChemie-InternationalEdition,2020,vol.59,p.8880-8884    Angew.Chem.,2020,vol.132,p.8965-8969,5

[10]JournaloftheAmericanChemicalSociety,1969,vol.91,p.6464-6470

[11]JournalofOrganicChemistry,2002,vol.67,p.9428-9438

[12]JournalofMedicinalChemistry,2002,vol.45,p.2319-2324

[13]Patent:US5886022,1999,A

[14]OrganicLetters,2011,vol.13,p.1572-1575

[15]Synthesis,2013,vol.45,p.545-555

[16]AngewandteChemie-InternationalEdition,2017,vol.56,p.7863-7866    Angew.Chem.,2017,vol.129,p.7971-7974,4

[17]Chemistry-AEuropeanJournal,2017,vol.23,p.12763-12766

[18]OrganicLetters,2017,vol.19,p.5856-5859

[19]Chemistry-AEuropeanJournal,2018,vol.24,p.1606-1618

[20]ChemicalCommunications,2018,vol.54,p.2040-2043

[21]OrganicLetters,2018,vol.20,p.6534-6538

[22]OrganicLetters,2019,vol.21,p.5295-5300

[1]JournaloftheChemicalSociety.PerkintransactionsI,1987,p.2321-2332

[1]JournaloftheChemicalSociety.PerkintransactionsI,1987,p.2321-2332

627-19-0    26059-40-5   
2-(pent-1-ynylphenyl)ethanol 

[1]ChemicalCommunications,2011,vol.47,p.7992-7994

[2]OrganicLetters,2005,vol.7,p.5437-5440

Literature

Title: Bioconversion of iodoacetophenones by marine fungi.

Journal: Marine biotechnology (New York, N.Y.) 20120801

Title: Radical deoxygenation of hydroxyl groups via phosphites.

Journal: Journal of the American Chemical Society 20041020

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SDS
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