4249-72-3,MFCD09880900
Catalog No.:AA00C6QC

4249-72-3 | 2-Phenoxy-1-phenylethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$15.00   $11.00
- +
5g
97%
in stock  
$31.00   $22.00
- +
10g
97%
in stock  
$56.00   $39.00
- +
25g
97%
in stock  
$135.00   $95.00
- +
100g
97%
in stock  
$474.00 $332.00
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00C6QC
Chemical Name:
2-Phenoxy-1-phenylethanol
CAS Number:
4249-72-3
Molecular Formula:
C14H14O2
Molecular Weight:
214.2598
MDL Number:
MFCD09880900
SMILES:
OC(c1ccccc1)COc1ccccc1
Properties
Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.7  

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1951,vol.16,p.1809

[2]ChemicalCommunications,2006,p.4315-4317

[3]JournalofOrganicChemistry,2003,vol.68,p.726-730

[4]AdvancedSynthesisandCatalysis,2010,vol.352,p.2489-2496

[5]TetrahedronLetters,2013,vol.54,p.5099-5102

[1]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[2]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[3]GreenChemistry,2016,vol.18,p.6229-6235

[4]DaltonTransactions,2017,vol.46,p.11884-11889

[5]GreenChemistry,2019,vol.21,p.2005-2014

[6]CatalysisToday,2016,vol.269,p.40-47

[7]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[8]ChemicalCommunications,2015,vol.51,p.4028-4031

[9]ACSCatalysis,2016,vol.6,p.1316-1328

[10]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[11]TetrahedronLetters,2010,vol.51,p.6418-6421

[12]ChemicalCommunications,2019,vol.55,p.13144-13147

[13]GreenChemistry,2020,vol.22,p.248-255

[14]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0101

[15]GreenChemistry,2014,vol.16,p.2432-2437

[16]JournaloftheAmericanChemicalSociety,1958,vol.80,p.202

[17]JournaloftheChemicalSociety,1960,p.3521-3527

[18]JournaloftheChemicalSociety.PerkintransactionsII,1978,p.1135-1144

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1990,vol.271,p.927-930

[20]JournalofOrganicChemistry,2006,vol.71,p.7035-7044

[21]JournalofOrganicChemistry,2002,vol.67,p.7937-7945

[22]Tetrahedron,2008,vol.64,p.3867-3876

[23]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[24]ChemicalCommunications,2015,vol.51,p.12212-12215

[25]GreenChemistry,2015,vol.17,p.5009-5018

[26]GreenChemistry,2016,vol.18,p.2029-2036

[27]GreenChemistry,2016,vol.18,p.6545-6555

[28]GreenChemistry,2019,vol.21,p.1974-1981

[29]GreenChemistry,2019,vol.21,p.6707-6716

[1]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[2]RSCAdvances,2016,vol.6,p.104742-104753

[3]ChemSusChem,2020,vol.13,p.1740-1745

[4]ChemCatChem,2015,vol.7,p.401-404

[5]GreenChemistry,2016,vol.18,p.2029-2036

[6]ACSCatalysis,2016,vol.6,p.6086-6090

[7]ChemicalCommunications,2019,vol.55,p.14143-14146

[8]TetrahedronLetters,2016,vol.57,p.3024-3028

[9]CanadianJournalofChemistry,1995,vol.73,p.2079-2085

[10]AngewandteChemie-InternationalEdition,2013,vol.52,p.12674-12678    Angew.Chem.,2013,vol.125,p.12906-12910

[11]InorganicChemistry,2014,vol.53,p.11377-11387

[12]GreenChemistry,2015,vol.17,p.5009-5018

[13]ACSCatalysis,2017,vol.7,p.4571-4580

[14]ACSCatalysis,2017,vol.7,p.3419-3429

[15]ChemCatChem,2019,vol.11,p.3786-3790

[16]GreenChemistry,2019,vol.21,p.2005-2014

[17]ACSCatalysis,2019,vol.9,p.11341-11349

[18]ACSCatalysis,2019,vol.9,p.11341-11349

[19]GreenChemistry,2020,vol.22,p.248-255

[1]Patent:US2006/89415,2006,A1.Locationinpatent:Page/Pagecolumn11

[1]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[2]GreenChemistry,2017,vol.19,p.4538-4543

[3]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[4]GreenChemistry,2016,vol.18,p.6545-6555

Literature

Title: Effects of the antimycobacterial compound 2-phenoxy-1-phenylethanone on rat hepatocytes and formation of metabolites.

Journal: Pharmaceutical biology 20121001

Title: Aerobic oxidation of lignin models using a base metal vanadium catalyst.

Journal: Inorganic chemistry 20100621

Title: Model compound studies of the beta-O-4 linkage in lignin: absolute rate expressions for beta-scission of phenoxyl radical from 1-phenyl-2-phenoxyethanol-1-yl radical.

Journal: The Journal of organic chemistry 20021115

Quotation Request
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Additional Info:
SDS
Tags:4249-72-3 Molecular Formula|4249-72-3 MDL|4249-72-3 SMILES|4249-72-3 2-Phenoxy-1-phenylethanol
Catalog No.: AA00C6QC
4249-72-3,MFCD09880900
4249-72-3 | 2-Phenoxy-1-phenylethanol
Pack Size: 250mg
Purity: 97%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 97%
in stock
$15.00 $11.00
Pack Size: 5g
Purity: 97%
in stock
$31.00 $22.00
Pack Size: 10g
Purity: 97%
in stock
$56.00 $39.00
Pack Size: 25g
Purity: 97%
in stock
$135.00 $95.00
Pack Size: 100g
Purity: 97%
in stock
$474.00 $332.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00C6QC
Chemical Name: 2-Phenoxy-1-phenylethanol
CAS Number: 4249-72-3
Molecular Formula: C14H14O2
Molecular Weight: 214.2598
MDL Number: MFCD09880900
SMILES: OC(c1ccccc1)COc1ccccc1
Properties
Complexity: 181  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.7  
Downstream Synthesis Route
96-09-3    108-95-2    4249-72-3    53574-80-4 

[1]JournalofOrganicChemistry,1951,vol.16,p.1809

[2]ChemicalCommunications,2006,p.4315-4317

[3]JournalofOrganicChemistry,2003,vol.68,p.726-730

[4]AdvancedSynthesisandCatalysis,2010,vol.352,p.2489-2496

[5]TetrahedronLetters,2013,vol.54,p.5099-5102

721-04-0    4249-72-3 

[1]Chemistry-AEuropeanJournal,2020,vol.26,p.3641-3646

[2]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[3]GreenChemistry,2016,vol.18,p.6229-6235

[4]DaltonTransactions,2017,vol.46,p.11884-11889

[5]GreenChemistry,2019,vol.21,p.2005-2014

[6]CatalysisToday,2016,vol.269,p.40-47

[7]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[8]ChemicalCommunications,2015,vol.51,p.4028-4031

[9]ACSCatalysis,2016,vol.6,p.1316-1328

[10]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[11]TetrahedronLetters,2010,vol.51,p.6418-6421

[12]ChemicalCommunications,2019,vol.55,p.13144-13147

[13]GreenChemistry,2020,vol.22,p.248-255

[14]Patent:US2016/52949,2016,A1.Locationinpatent:Paragraph0101

[15]GreenChemistry,2014,vol.16,p.2432-2437

[16]JournaloftheAmericanChemicalSociety,1958,vol.80,p.202

[17]JournaloftheChemicalSociety,1960,p.3521-3527

[18]JournaloftheChemicalSociety.PerkintransactionsII,1978,p.1135-1144

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1990,vol.271,p.927-930

[20]JournalofOrganicChemistry,2006,vol.71,p.7035-7044

[21]JournalofOrganicChemistry,2002,vol.67,p.7937-7945

[22]Tetrahedron,2008,vol.64,p.3867-3876

[23]JournalofOrganicChemistry,2011,vol.76,p.1883-1886

[24]ChemicalCommunications,2015,vol.51,p.12212-12215

[25]GreenChemistry,2015,vol.17,p.5009-5018

[26]GreenChemistry,2016,vol.18,p.2029-2036

[27]GreenChemistry,2016,vol.18,p.6545-6555

[28]GreenChemistry,2019,vol.21,p.1974-1981

[29]GreenChemistry,2019,vol.21,p.6707-6716

4249-72-3    721-04-0 

[1]EuropeanJournalofInorganicChemistry,2019,vol.2019,p.4637-4646

[2]RSCAdvances,2016,vol.6,p.104742-104753

[3]ChemSusChem,2020,vol.13,p.1740-1745

[4]ChemCatChem,2015,vol.7,p.401-404

[5]GreenChemistry,2016,vol.18,p.2029-2036

[6]ACSCatalysis,2016,vol.6,p.6086-6090

[7]ChemicalCommunications,2019,vol.55,p.14143-14146

[8]TetrahedronLetters,2016,vol.57,p.3024-3028

[9]CanadianJournalofChemistry,1995,vol.73,p.2079-2085

[10]AngewandteChemie-InternationalEdition,2013,vol.52,p.12674-12678    Angew.Chem.,2013,vol.125,p.12906-12910

[11]InorganicChemistry,2014,vol.53,p.11377-11387

[12]GreenChemistry,2015,vol.17,p.5009-5018

[13]ACSCatalysis,2017,vol.7,p.4571-4580

[14]ACSCatalysis,2017,vol.7,p.3419-3429

[15]ChemCatChem,2019,vol.11,p.3786-3790

[16]GreenChemistry,2019,vol.21,p.2005-2014

[17]ACSCatalysis,2019,vol.9,p.11341-11349

[18]ACSCatalysis,2019,vol.9,p.11341-11349

[19]GreenChemistry,2020,vol.22,p.248-255

4249-72-3    66694-17-5 

[1]Patent:US2006/89415,2006,A1.Locationinpatent:Page/Pagecolumn11

4249-72-3    74-88-4    29509-35-1 

[1]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12554-12555

[2]GreenChemistry,2017,vol.19,p.4538-4543

[3]JournaloftheAmericanChemicalSociety,2020,vol.142,p.4037-4050

[4]GreenChemistry,2016,vol.18,p.6545-6555

Literature fold

Title: Effects of the antimycobacterial compound 2-phenoxy-1-phenylethanone on rat hepatocytes and formation of metabolites.

Journal: Pharmaceutical biology20121001

Title: Aerobic oxidation of lignin models using a base metal vanadium catalyst.

Journal: Inorganic chemistry20100621

Title: Model compound studies of the beta-O-4 linkage in lignin: absolute rate expressions for beta-scission of phenoxyl radical from 1-phenyl-2-phenoxyethanol-1-yl radical.

Journal: The Journal of organic chemistry20021115

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