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18698-96-9,MFCD00046546
Catalog No.:AA0033AF

18698-96-9 | 2-Iodophenylacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$16.00   $11.00
- +
10g
97%
in stock  
$27.00   $19.00
- +
25g
97%
in stock  
$63.00   $44.00
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100g
97%
in stock  
$249.00   $174.00
- +
500g
97%
in stock  
$1,179.00   $826.00
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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:
AA0033AF
Chemical Name:
2-Iodophenylacetic acid
CAS Number:
18698-96-9
Molecular Formula:
C8H7IO2
Molecular Weight:
262.0445
MDL Number:
MFCD00046546
SMILES:
OC(=O)Cc1ccccc1I
Properties
Properties
 
BP:
344.5°C at 760 mmHg  
Form:
Solid  
MP:
116-119 °C(lit.)  
Stability:
Light Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
147  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.3  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1960,vol.25,p.424-428

[1]OrganicLetters,2017,vol.19,#7,p.1634-1637

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

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

[1]OrganicLetters,2005,vol.7,#22,p.4963-4966

[2]OrganicLetters,2008,vol.10,#21,p.4987-4990

[3]OrganicLetters,2009,vol.11,#1,p.229-231

[4]JournaloftheChemicalSociety,1941,p.487,489

[5]Synthesis(Germany),2015,vol.47,#13,p.1913-1921

Downstream Synthesis Route

[1]OrganicLetters,2005,vol.7,p.4963-4966

[2]OrganicLetters,2008,vol.10,p.4987-4990

[3]OrganicLetters,2009,vol.11,p.229-231

[4]JournaloftheChemicalSociety,1941,p.487,489

[5]Synthesis,2015,vol.47,p.1913-1921

[1]JournalofOrganicChemistry,1999,vol.64,p.4830-4833

[2]JournaloftheChemicalSociety,1941,p.487,489

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

[4]JournalofOrganicChemistry,1986,vol.51,p.4303-4307

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

[6]Synlett,2003,p.1603-1606

[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

3132-99-8    18698-96-9   
α-(o-iodophenyl)-m-bromocinnamicacid 

[1]Nesmeyanov,A.N.;Tolstaya,T.P.;Vanchikova,L.N.;Petrakov,A.V.[BulletinoftheAcademyofSciencesoftheUSSRDivisionofChemicalScience,1980,vol.29,p.1789-1792][IzvestiyaAkademiiNaukSSSR,SeriyaKhimicheskaya,1980,#11,p.2530-2534]

[2]Isobe,Hiroyuki;Nanjo,Yuki;Sato,Sota;Yang,Yong[Organicandbiomolecularchemistry,2020,vol.18,#26,p.4949-4955]

[1]Locationinpatent:experimentalpartVischer,HenryF.;Hulshof,JannekeW.;Hulscher,Saskia;Fratantoni,SilvinaA.;Verheij,MarkH.P.;Victorina,Jane;Smit,MartineJ.;deEsch,IwanJ.P.;Leurs,Rob[BioorganicandMedicinalChemistry,2010,vol.18,#2,p.675-688]

[2]Jilek;Pomykacek;Dlabac;etal.[CollectionofCzechoslovakChemicalCommunications,1980,vol.45,#2,p.504-516]

[3]Boudhar,Aicha;Ng,XiaoWei;Loh,ChiewYee;Chia,WanNi;Tan,ZhiMing;Nosten,Francois;Dymock,BrianW.;Tan,KevinS.W.[EuropeanJournalofMedicinalChemistry,2016,vol.119,p.231-249]

Literature

Title: Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors.

Journal: The open medicinal chemistry journal 20090101

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