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60-12-8,MFCD00002886
Catalog No.:AA0033CN

60-12-8 | 2-Phenylethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
95%
in stock  
$8.00   $6.00
- +
100g
95%
in stock  
$11.00   $8.00
- +
500g
95%
in stock  
$22.00   $15.00
- +
  • 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:
AA0033CN
Chemical Name:
2-Phenylethanol
CAS Number:
60-12-8
Molecular Formula:
C8H10O
Molecular Weight:
122.1644
MDL Number:
MFCD00002886
SMILES:
OCCc1ccccc1
FEMA Number:
2858
UN Number:
2810
Properties
Properties
 
BP:
219-221 °C750 mm Hg(lit.)  
Form:
Liquid  
MP:
−27 °C(lit.)  
Refractive Index:
n20/D 1.5317(lit.)  
Solubility:
Miscible with chloroform.  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
65  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1.4  

Upstream Synthesis Route

[1]ACSCatalysis,2016,vol.6,#12,p.8162-8165

[2]RussianChemicalBulletin,2015,vol.64,#9,p.2210-2214

[3]Izv.Akad.Nauk,Ser.Khim.,2015,#9,p.2210-2214,5

[1]ChemicalandPharmaceuticalBulletin,1988,vol.36,#10,p.4244-4247

[1]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1980,vol.16,#11,p.1153-1156

[2]KhimiyaGeterotsiklicheskikhSoedinenii,1980,vol.16,#11,p.1516-1519

[1]JournalofMolecularCatalysisB:Enzymatic,2012,vol.84,p.121-127

[1]JournalofMolecularCatalysisB:Enzymatic,2010,vol.66,#1-2,p.72-80

Downstream Synthesis Route

[1]TetrahedronLetters,2005,vol.46,p.1651-1653

[2]ChemistryLetters,1983,p.1097-1100

[3]BulletinoftheChemicalSocietyofJapan,1992,vol.65,p.703-706

[4]ChemicalCommunications,2019,vol.55,p.2797-2800

[5]JournalofOrganicChemistry,1987,vol.52,p.4319-4327

[6]CatalysisCommunications,2013,vol.40,p.80-83

[7]TetrahedronLetters,2016,vol.57,p.2873-2876

[8]ChemischeBerichte,1900,vol.33,p.1723

[9]TetrahedronLetters,1981,vol.22,p.5327-5330

[10]JournalofOrganicChemistry,1983,vol.48,p.1286-1292

[11]BulletinoftheChemicalSocietyofJapan,1989,vol.62,p.2585-2588

[12]TetrahedronLetters,2006,vol.47,p.9199-9201

[13]JournaloftheAmericanChemicalSociety,2008,vol.130,p.17672-17673

[14]AdvancedSynthesisandCatalysis,2012,vol.354,p.3045-3053

[15]JournalofOrganicChemistry,2013,vol.78,p.6593-6598

[16]Organometallics,2019,vol.38,p.1750-1760

[1]ChemistryLetters,1980,p.927-930

[2]JournaloftheChemicalSociety.Chemicalcommunications,1979,p.303-304

[1]ChemicalandPharmaceuticalBulletin,1983,vol.31,p.3946-3950

[1]JournalofHeterocyclicChemistry,1987,vol.24,p.1203-1204

60-12-8    13827-62-8   
Naphthalene-2,6-disulfonicaciddiphenethylester 

[1]Heterocycles,1993,vol.36,p.1715-1720

Literature

Title: Lingappa BT, et al. Phenethyl alcohol and tryptophol: autoantibiotics produced by the fungus Candida albicans. Science. 1969 Jan 10;163(3863):192-4.

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SDS
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