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1878-94-0,MFCD00014359
Catalog No.:AA002GG4

1878-94-0 | 4-Iodophenoxyacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$18.00   $13.00
- +
25g
95%
in stock  
$40.00   $28.00
- +
100g
95%
in stock  
$127.00   $89.00
- +
500g
95%
in stock  
$445.00   $312.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002GG4
Chemical Name:
4-Iodophenoxyacetic acid
CAS Number:
1878-94-0
Molecular Formula:
C8H7IO3
Molecular Weight:
278.0439
MDL Number:
MFCD00014359
SMILES:
OC(=O)COc1ccc(cc1)I
Properties
Properties
 
BP:
358.5°C at 760 mmHg  
Form:
Solid  
MP:
154-157 °C(lit.)  
Stability:
Light Sensitive  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
152  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.7  

Upstream Synthesis Route

[1]JournalofOrganometallicChemistry,2013,vol.747,p.189-194

[2]JournalofMedicinalChemistry,2007,vol.50,#7,p.1675-1684

[3]BioorganicandMedicinalChemistryLetters,2010,vol.20,#4,p.1453-1456

[4]Patent:WO2007/120012,2007,A1,.Locationinpatent:Page/Pagecolumn79

[1]JournalofMolecularStructure,2014,vol.1074,p.487-495

[2]GazzettaChimicaItaliana,1920,vol.50I,p.183

[3]BioorganicChemistry,2015,vol.59,p.151-167

[1]ChemCatChem,2018,vol.10,#2,p.376-380

[2]Austral.J.scient.Res.,1949,vol.<A>2,p.246

[3]GazzettaChimicaItaliana,1920,vol.50I,p.183

[1]Luminescence,2014,vol.29,#8,p.1113-1122

[1]TetrahedronLetters,2004,vol.45,#42,p.7911-7914

[2]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1982,vol.21,#2,p.154-156

Downstream Synthesis Route

[1]DokladyAkademiiNaukSSSR,1954,vol.97,p.255    Chem.Abstr.,1955,p.8846

[1]GazzettaChimicaItaliana,1920,vol.50I,p.183

[1]Patent:BE854683,1977,    Chem.Abstr.,1978,vol.89

[2]Patent:DE2623228,1977,    Chem.Abstr.,1978,vol.88

[1]JournalofMedicinalChemistry,2018,vol.61,p.10545-10557

[2]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1981,vol.20,p.629-631

[3]JournaloftheIndianChemicalSociety,1981,vol.58,p.1082-1083

[1]PharmaceuticalChemistryJournal,1986,vol.20,p.555-558    Khimiko-FarmatsevticheskiiZhurnal,1986,vol.20,p.952-956

Literature

Title: Efficient synthesis of p-quinols using catalytic hypervalent iodine oxidation of 4-arylphenols with 4-iodophenoxyacetic acid and oxone.

Journal: Chemical & pharmaceutical bulletin 20090601

Title: Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and oxone: oxidation of p-alkoxyphenols to p-benzoquinones.

Journal: Chemical & pharmaceutical bulletin 20090301

Title: Catalytic hypervalent iodine oxidation of p-dialkoxybenzenes to p-quinones using 4-iodophenoxyacetic acid and Oxone.

Journal: Chemical & pharmaceutical bulletin 20081101

Quotation Request
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SDS
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Tags:1878-94-0 Molecular Formula|1878-94-0 MDL|1878-94-0 SMILES|1878-94-0 4-Iodophenoxyacetic acid
Catalog No.: AA002GG4
1878-94-0,MFCD00014359
1878-94-0 | 4-Iodophenoxyacetic acid
Pack Size： 5g
Purity： 95%
in stock
$18.00 $13.00
Pack Size： 25g
Purity： 95%
in stock
$40.00 $28.00
Pack Size： 100g
Purity： 95%
in stock
$127.00 $89.00
Pack Size： 500g
Purity： 95%
in stock
$445.00 $312.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002GG4
Chemical Name: 4-Iodophenoxyacetic acid
CAS Number: 1878-94-0
Molecular Formula: C8H7IO3
Molecular Weight: 278.0439
MDL Number: MFCD00014359
SMILES: OC(=O)COc1ccc(cc1)I
Properties
BP: 358.5°C at 760 mmHg  
Form: Solid  
MP: 154-157 °C(lit.)  
Stability: Light Sensitive  
Storage: Keep in dry area;2-8℃;  
Complexity: 152  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 2.7  
Upstream Synthesis Route
90794-33-5    1878-94-0 

[1]JournalofOrganometallicChemistry,2013,vol.747,p.189-194

[2]JournalofMedicinalChemistry,2007,vol.50,#7,p.1675-1684

[3]BioorganicandMedicinalChemistryLetters,2010,vol.20,#4,p.1453-1456

[4]Patent:WO2007/120012,2007,A1,.Locationinpatent:Page/Pagecolumn79

540-38-5    79-11-8    1878-94-0 

[1]JournalofMolecularStructure,2014,vol.1074,p.487-495

[2]GazzettaChimicaItaliana,1920,vol.50I,p.183

[3]BioorganicChemistry,2015,vol.59,p.151-167

122-59-8    1878-94-0 

[1]ChemCatChem,2018,vol.10,#2,p.376-380

[2]Austral.J.scient.Res.,1949,vol.<A>2,p.246

[3]GazzettaChimicaItaliana,1920,vol.50I,p.183

540-38-5    3926-62-3    1878-94-0 

[1]Luminescence,2014,vol.29,#8,p.1113-1122

81720-18-5    1878-94-0 

[1]TetrahedronLetters,2004,vol.45,#42,p.7911-7914

[2]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1982,vol.21,#2,p.154-156

Downstream Synthesis Route
2298-36-4    1878-94-0 

[1]DokladyAkademiiNaukSSSR,1954,vol.97,p.255    Chem.Abstr.,1955,p.8846

1878-94-0    113305-56-9 

[1]GazzettaChimicaItaliana,1920,vol.50I,p.183

364-62-5    1878-94-0    65569-50-8 

[1]Patent:BE854683,1977,    Chem.Abstr.,1978,vol.89

[2]Patent:DE2623228,1977,    Chem.Abstr.,1978,vol.88

67-56-1    1878-94-0    81720-18-5 

[1]JournalofMedicinalChemistry,2018,vol.61,p.10545-10557

[2]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1981,vol.20,p.629-631

[3]JournaloftheIndianChemicalSociety,1981,vol.58,p.1082-1083

102-71-6    1878-94-0    87385-58-8 

[1]PharmaceuticalChemistryJournal,1986,vol.20,p.555-558    Khimiko-FarmatsevticheskiiZhurnal,1986,vol.20,p.952-956

Literature fold

Title: Efficient synthesis of p-quinols using catalytic hypervalent iodine oxidation of 4-arylphenols with 4-iodophenoxyacetic acid and oxone.

Journal: Chemical & pharmaceutical bulletin20090601

Title: Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and oxone: oxidation of p-alkoxyphenols to p-benzoquinones.

Journal: Chemical & pharmaceutical bulletin20090301

Title: Catalytic hypervalent iodine oxidation of p-dialkoxybenzenes to p-quinones using 4-iodophenoxyacetic acid and Oxone.

Journal: Chemical & pharmaceutical bulletin20081101

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