Home Fluorides 368-63-8
368-63-8,MFCD01632521
Catalog No.:AA003DQJ

368-63-8 | 1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-ol

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Purity
Availability
Price(USD)
Quantity
  
10g
95%
in stock  
$112.00   $78.00
- +
25g
95%
in stock  
$278.00   $195.00
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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:
AA003DQJ
Chemical Name:
1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-ol
CAS Number:
368-63-8
Molecular Formula:
C10H8F6O
Molecular Weight:
258.1603
MDL Number:
MFCD01632521
SMILES:
CC(c1cc(cc(c1)C(F)(F)F)C(F)(F)F)O
Properties
Properties
 
BP:
175.8°C at 760 mmHg  
Form:
Solid  
MP:
70-74℃  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
237  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
3.2  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,2003,vol.68,#11,p.4600-4603

[1]Patent:EP2597079,2013,A1,

[2]RSCAdvances,2015,vol.5,#57,p.45943-45955

[1]OrganicLetters,2003,vol.5,#23,p.4249-4251

[2]JournaloftheAmericanChemicalSociety,1990,vol.112,#15,p.5741-5747

[3]JournalofCatalysis,2004,vol.222,#1,p.117-128

[4]TetrahedronAsymmetry,2003,vol.14,#22,p.3581-3587

[5]AngewandteChemie(Internationaled.inEnglish),2004,vol.43,#21,p.2816-2819

[6]TetrahedronAsymmetry,2004,vol.15,#21,p.3413-3418

[7]AdvancedSynthesisandCatalysis,2005,vol.347,#9,p.1193-1197

[8]AdvancedSynthesisandCatalysis,2006,vol.348,#1-2,p.47-50

[9]OrganicLetters,2006,vol.8,#14,p.2969-2972

[10]JournalofOrganometallicChemistry,2006,vol.691,#10,p.2332-2334

[11]TetrahedronAsymmetry,2006,vol.17,#13,p.2000-2005

[12]Tetrahedron,2004,vol.60,#3,p.789-797

[13]TetrahedronAsymmetry,2007,vol.18,#10,p.1224-1232

[14]Patent:WO2006/67395,2006,A1,.Locationinpatent:Page/Pagecolumn20-21

[15]Patent:WO2006/67395,2006,A1,.Locationinpatent:Page/Pagecolumn25-26

[16]Patent:WO2006/67395,2006,A1,.Locationinpatent:Page/Pagecolumn25

[17]Patent:WO2006/67395,2006,A1,.Locationinpatent:Page/Pagecolumn24-25

[18]Patent:WO2006/67395,2006,A1,.Locationinpatent:Page/Pagecolumn24-25

[19]Patent:WO2006/54115,2006,A1,.Locationinpatent:Page/Pagecolumn9-10

[20]Patent:WO2006/54115,2006,A1,.Locationinpatent:Page/Pagecolumn9-10

[21]Patent:WO2006/54115,2006,A1,.Locationinpatent:Page/Pagecolumn9-10

[22]Patent:EP1927596,2008,A1,.Locationinpatent:Page/Pagecolumn32

[23]AdvancedSynthesisandCatalysis,2008,vol.350,#1,p.197-204

[24]JournalofOrganometallicChemistry,2008,vol.693,#23,p.3527-3532

[25]TetrahedronAsymmetry,2009,vol.20,#23,p.2759-2763

[26]Patent:US2010/261924,2010,A1,.Locationinpatent:Page/Pagecolumn89;91

[27]TetrahedronLetters,2009,vol.50,#6,p.688-692

[28]OrganicandBiomolecularChemistry,2011,vol.9,#16,p.5652-5654

[29]OrganicandBiomolecularChemistry,2012,vol.10,#2,p.355-360

[30]Patent:WO2012/31358,2012,A1,.Locationinpatent:Page/Pagecolumn56;70

[31]OrganicProcessResearchandDevelopment,2012,vol.16,#4,p.710-713

[32]MonatsheftefurChemie,2012,vol.143,#7,p.1045-1054

[33]Chemistry-AnAsianJournal,2012,vol.7,#11,p.2527-2530,4

[34]Chemistry-AnAsianJournal,2012,vol.7,#11,p.2527-2530

[35]AdvancedSynthesisandCatalysis,2012,vol.354,#13,p.2545-2555,11

[36]AdvancedSynthesisandCatalysis,2012,vol.354,#13,p.2545-2555

[37]AngewandteChemie-InternationalEdition,2012,vol.51,#46,p.11624-11628

[38]Angew.Chem.,2012,vol.124,#46,p.11792-11796,5

[39]ChemCatChem,2013,vol.5,#8,p.2253-2257

[40]OrganicLetters,2013,vol.15,#19,p.5110-5113

[41]OrganicProcessResearchandDevelopment,2007,vol.11,#3,p.519-523

[42]JournalofMolecularCatalysisB:Enzymatic,2014,vol.102,p.1-8

[43]JournalofMolecularCatalysisB:Enzymatic,2014,vol.102,p.1-8

[44]Patent:WO2014/68331,2014,A1,.Locationinpatent:Page/Pagecolumn82

[45]OrganicProcessResearchandDevelopment,2014,vol.18,#6,p.793-800

[46]CatalysisCommunications,2014,vol.57,p.111-114

[47]CatalysisCommunications,2014,vol.57,p.111-114

[48]JournalofOrganometallicChemistry,2014,vol.771,p.2-8

[49]JournalofOrganometallicChemistry,2014,vol.771,p.2-8

[50]Organometallics,2014,vol.33,#19,p.5517-5524

[51]Organometallics,2014,vol.33,#19,p.5517-5524

[52]Organometallics,2014,vol.33,#20,p.5791-5801

[53]OrganicProcessResearchandDevelopment,2014,vol.18,#9,p.1137-1141

[54]JournalofMolecularCatalysisA:Chemical,2016,vol.411,p.196-202

[55]RSCAdvances,2016,vol.6,#91,p.88580-88587

[56]ACSCatalysis,2016,vol.6,#10,p.6455-6464

[57]Patent:CN103232324,2016,B,.Locationinpatent:Paragraph0086-0093

[58]Chemistry-AEuropeanJournal,2017,vol.23,#30,p.7212-7216

[59]ChemicalScience,2017,vol.8,#9,p.6531-6541

[60]ChemCatChem,2017,vol.9,#16,p.3125-3130

[61]ACSCatalysis,2017,vol.7,#10,p.6827-6842

[62]ProcessBiochemistry,2017,vol.57,p.72-79

[63]Organometallics,2018,vol.37,#3,p.491-504

[64]EuropeanJournalofOrganicChemistry,2018,vol.2018,#23,p.3031-3035

[65]OrganicLetters,2018,vol.20,#19,p.6135-6139

[66]Organometallics,2018,vol.37,#24,p.4608-4618

[1]JournalofOrganicChemistry,2003,vol.68,#11,p.4600-4603

[1]RSCAdvances,2015,vol.5,#57,p.45943-45955

[2]ChemistryLetters,2005,vol.34,#8,p.1102-1103

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2019

[2]OrganicLetters,2003,vol.5,p.4249-4251

[3]JournaloftheAmericanChemicalSociety,1990,vol.112,p.5741-5747

[4]JournalofCatalysis,2004,vol.222,p.117-128

[5]TetrahedronAsymmetry,2003,vol.14,p.3581-3587

[6]AngewandteChemie-InternationalEditioninEnglish,2004,vol.43,p.2816-2819

[7]TetrahedronAsymmetry,2004,vol.15,p.3413-3418

[8]AdvancedSynthesisandCatalysis,2005,vol.347,p.1193-1197

[9]AdvancedSynthesisandCatalysis,2006,vol.348,p.47-50

[10]OrganicLetters,2006,vol.8,p.2969-2972

[11]JournalofOrganometallicChemistry,2006,vol.691,p.2332-2334

[12]TetrahedronAsymmetry,2006,vol.17,p.2000-2005

[13]Tetrahedron,2004,vol.60,p.789-797

[14]TetrahedronAsymmetry,2007,vol.18,p.1224-1232

[15]Patent:WO2006/67395,2006,A1.Locationinpatent:Page/Pagecolumn20-21

[16]Patent:WO2006/67395,2006,A1.Locationinpatent:Page/Pagecolumn25-26

[17]Patent:WO2006/67395,2006,A1.Locationinpatent:Page/Pagecolumn25

[18]Patent:WO2006/67395,2006,A1.Locationinpatent:Page/Pagecolumn24-25

[19]Patent:WO2006/67395,2006,A1.Locationinpatent:Page/Pagecolumn24-25

[20]Patent:WO2006/54115,2006,A1.Locationinpatent:Page/Pagecolumn9-10

[21]Patent:WO2006/54115,2006,A1.Locationinpatent:Page/Pagecolumn9-10

[22]Patent:WO2006/54115,2006,A1.Locationinpatent:Page/Pagecolumn9-10

[23]Patent:EP1927596,2008,A1.Locationinpatent:Page/Pagecolumn32

[24]AdvancedSynthesisandCatalysis,2008,vol.350,p.197-204

[25]JournalofOrganometallicChemistry,2008,vol.693,p.3527-3532

[26]TetrahedronAsymmetry,2009,vol.20,p.2759-2763

[27]Patent:US2010/261924,2010,A1.Locationinpatent:Page/Pagecolumn89;91

[28]TetrahedronLetters,2009,vol.50,p.688-692

[29]OrganicandBiomolecularChemistry,2011,vol.9,p.5652-5654

[30]OrganicandBiomolecularChemistry,2012,vol.10,p.355-360

[31]Patent:WO2012/31358,2012,A1.Locationinpatent:Page/Pagecolumn56;70

[32]OrganicProcessResearchandDevelopment,2012,vol.16,p.710-713

[33]MonatsheftefurChemie,2012,vol.143,p.1045-1054

[34]Chemistry-AnAsianJournal,2012,vol.7,p.2527-2530,4

[35]Advancedsynthesisandcatalysis,2012,vol.354,p.2545-2555,11

[36]AngewandteChemie-InternationalEdition,2012,vol.51,p.11624-11628    Angew.Chem.,2012,vol.124,p.11792-11796,5

[37]ChemCatChem,2013,vol.5,p.2253-2257

[38]OrganicLetters,2013,vol.15,p.5110-5113

[39]OrganicProcessResearchandDevelopment,2007,vol.11,p.519-523

[40]JournalofMolecularCatalysisB:Enzymatic,2014,vol.102,p.1-8

[41]JournalofMolecularCatalysisB:Enzymatic,2014,vol.102,p.1-8

[42]Patent:WO2014/68331,2014,A1.Locationinpatent:Page/Pagecolumn82

[43]OrganicProcessResearchandDevelopment,2014,vol.18,p.793-800

[44]CatalysisCommunications,2014,vol.57,p.111-114

[45]CatalysisCommunications,2014,vol.57,p.111-114

[46]JournalofOrganometallicChemistry,2014,vol.771,p.2-8

[47]JournalofOrganometallicChemistry,2014,vol.771,p.2-8

[48]Organometallics,2014,vol.33,p.5517-5524

[49]Organometallics,2014,vol.33,p.5517-5524

[50]Organometallics,2014,vol.33,p.5791-5801

[51]OrganicProcessResearchandDevelopment,2014,vol.18,p.1137-1141

[52]JournalofMolecularCatalysisA:Chemical,2016,vol.411,p.196-202

[53]RSCAdvances,2016,vol.6,p.88580-88587

[54]ACSCatalysis,2016,vol.6,p.6455-6464

[55]Patent:CN103232324,2016,B.Locationinpatent:Paragraph0086-0093

[56]Chemistry-AEuropeanJournal,2017,vol.23,p.7212-7216

[57]ChemicalScience,2017,vol.8,p.6531-6541

[58]ChemCatChem,2017,vol.9,p.3125-3130

[59]ACSCatalysis,2017,vol.7,p.6827-6842

[60]ProcessBiochemistry,2017,vol.57,p.72-79

[61]Organometallics,2018,vol.37,p.491-504

[62]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.3031-3035

[63]OrganicLetters,2018,vol.20,p.6135-6139

[64]Organometallics,2018,vol.37,p.4608-4618

[65]ChemCatChem,2019,vol.11,p.820-830

[66]AngewandteChemie-InternationalEdition,2019,vol.58,p.4973-4977    Angew.Chem.,2019,vol.131,p.5027-5031,5

[67]AdvancedSynthesisandCatalysis,2019,vol.361,p.4691-4706

[68]Patent:CN110590859,2019,A.Locationinpatent:Paragraph0063-0066;0069-0083

[69]AngewandteChemie-InternationalEdition,2020,vol.59,p.4498-4504    Angew.Chem.,2020,vol.132,p.4528-4534,7

[1]JournalofOrganicChemistry,2003,vol.68,p.4600-4603

[2]ChemicalCommunications,2019,vol.55,p.15033-15036

[1]RSCAdvances,2015,vol.5,p.45943-45955

[2]ChemistryLetters,2005,vol.34,p.1102-1103

[1]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[2]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[3]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[4]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[5]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[6]JournaloftheAmericanChemicalSociety,2003,vol.125,p.2129-2135

[7]JournalofOrganicChemistry,2002,vol.67,p.6743-6747

borane-THF 
  22348-32-9    30071-93-3    368-63-8 

[1]Patent:US2004/23960,2004,A1

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Tags:368-63-8 Molecular Formula|368-63-8 MDL|368-63-8 SMILES|368-63-8 1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-ol