60646-30-2,MFCD00062968
Catalog No.:AA003CDC

60646-30-2 | (S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
>99.0%(GC)
in stock  
$603.00   $422.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003CDC
Chemical Name:
(S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethanol
CAS Number:
60646-30-2
Molecular Formula:
C16H11F3O
Molecular Weight:
276.2531
MDL Number:
MFCD00062968
SMILES:
O[C@H](C(F)(F)F)c1c2ccccc2cc2c1cccc2
Properties
Properties
 
BP:
423.1°C at 760 mmHg  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
319  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
5  

Downstream Synthesis Route

[1]OrganicLetters,2002,vol.4,p.4139-4142

[2]JournalofOrganicChemistry,1991,vol.56,p.893-896

[1]JournalofOrganicChemistry,1991,vol.56,p.893-896

[2]Tetrahedron,1993,vol.49,p.1725-1738

[3]SyntheticCommunications,1998,vol.28,p.99-108

[4]JournalofOrganicChemistry,1999,vol.64,p.8794-8800

[1]JournaloftheChemicalSociety.Chemicalcommunications,1995,p.301-302

[2]Patent:EP907663,2004,B1.Locationinpatent:Page8;10;12

[3]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn16

[4]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn17-18

[5]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[6]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[7]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[8]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-8

[9]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-9

[10]Patent:US7683167,2010,B2.Locationinpatent:Page/Pagecolumn7;8;9

[11]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9;11

[12]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn10-11

[13]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9-11

[14]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn11

[15]Chirality,2012,vol.24,p.329-338

[16]AsianJournalofChemistry,2012,vol.24,p.4917-4922

[17]Chirality,2013,vol.25,p.54-58

[18]BulletinoftheKoreanChemicalSociety,2013,vol.34,p.2623-2628

[19]Chirality,2015,vol.27,p.518-522

[20]Chirality,2015,vol.27,p.507-517

[21]Chirality,2015,vol.27,p.500-506

[22]ChemistryLetters,2015,vol.44,p.946-948

[23]ChemistryLetters,2015,vol.44,p.1479-1481

[24]Chirality,2016,vol.28,p.340-346

[25]Molecules,2016,vol.21

[26]Molecules,2016,vol.21

[27]Molecules,2016,vol.21

[28]ChemicalCommunications,2017,vol.53,p.509-512

[29]Chirality,2017,vol.29,p.430-442

[30]Chirality,2017,vol.29,p.512-521

[31]Chirality,2018,vol.30,p.74-84

[32]BulletinoftheKoreanChemicalSociety,2019,vol.40,p.146-149

[33]JournaloftheAmericanChemicalSociety,2019

108-24-7    60646-30-2   
(S)-1-(9-anthryl)-2,2,2-trifluoroethylacetate 

[1]BulletinoftheChemicalSocietyofJapan,1996,vol.69,p.1755-1761

60646-30-2   
di(S)-1-(9-anthryl)-2,2,2-trifluoroethylsulphite 

[1]TetrahedronAsymmetry,2001,vol.12,p.1737-1740

Literature

Title: Chemical profiling of the cytotoxic triterpenoid-concentrating fraction and characterization of ergostane stereo-isomer ingredients from Antrodia camphorata.

Journal: Journal of pharmaceutical and biomedical analysis 20120125

Title: Phosphorus-nitrogen compounds. 21. Syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclic phosphazene derivatives. The NMR behaviors of chiral phosphazenes with stereogenic centers upon the addition of chiral solvating agents.

Journal: Inorganic chemistry 20100802

Title: Phosphorus-nitrogen compounds. 18. Syntheses, stereogenic properties, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic mono- and bisferrocenylphosphazene derivatives.

Journal: Inorganic chemistry 20091102

Title: The structural and stereogenic properties of pentaerythritoxy-bridged cyclotriphosphazene derivatives: spiro-spiro, spiro-ansa and ansa-ansa isomers.

Journal: Dalton transactions (Cambridge, England : 2003) 20060314

Quotation Request
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Additional Info:
SDS
Historical Records
Tags:60646-30-2 Molecular Formula|60646-30-2 MDL|60646-30-2 SMILES|60646-30-2 (S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethanol
Catalog No.: AA003CDC
60646-30-2,MFCD00062968
60646-30-2 | (S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethanol
Pack Size: 1g
Purity: >99.0%(GC)
in stock
$603.00 $422.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003CDC
Chemical Name: (S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethanol
CAS Number: 60646-30-2
Molecular Formula: C16H11F3O
Molecular Weight: 276.2531
MDL Number: MFCD00062968
SMILES: O[C@H](C(F)(F)F)c1c2ccccc2cc2c1cccc2
Properties
BP: 423.1°C at 760 mmHg  
Storage: Keep in dry area;Room Temperature;  
Complexity: 319  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 5  
Downstream Synthesis Route
53531-31-0    60646-30-2 

[1]OrganicLetters,2002,vol.4,p.4139-4142

[2]JournalofOrganicChemistry,1991,vol.56,p.893-896

53531-31-0    60646-30-2    53531-34-3 

[1]JournalofOrganicChemistry,1991,vol.56,p.893-896

[2]Tetrahedron,1993,vol.49,p.1725-1738

[3]SyntheticCommunications,1998,vol.28,p.99-108

[4]JournalofOrganicChemistry,1999,vol.64,p.8794-8800

60686-64-8    60646-30-2    53531-34-3 

[1]JournaloftheChemicalSociety.Chemicalcommunications,1995,p.301-302

[2]Patent:EP907663,2004,B1.Locationinpatent:Page8;10;12

[3]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn16

[4]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn17-18

[5]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[6]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[7]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8

[8]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-8

[9]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-9

[10]Patent:US7683167,2010,B2.Locationinpatent:Page/Pagecolumn7;8;9

[11]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9;11

[12]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn10-11

[13]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9-11

[14]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn11

[15]Chirality,2012,vol.24,p.329-338

[16]AsianJournalofChemistry,2012,vol.24,p.4917-4922

[17]Chirality,2013,vol.25,p.54-58

[18]BulletinoftheKoreanChemicalSociety,2013,vol.34,p.2623-2628

[19]Chirality,2015,vol.27,p.518-522

[20]Chirality,2015,vol.27,p.507-517

[21]Chirality,2015,vol.27,p.500-506

[22]ChemistryLetters,2015,vol.44,p.946-948

[23]ChemistryLetters,2015,vol.44,p.1479-1481

[24]Chirality,2016,vol.28,p.340-346

[25]Molecules,2016,vol.21

[26]Molecules,2016,vol.21

[27]Molecules,2016,vol.21

[28]ChemicalCommunications,2017,vol.53,p.509-512

[29]Chirality,2017,vol.29,p.430-442

[30]Chirality,2017,vol.29,p.512-521

[31]Chirality,2018,vol.30,p.74-84

[32]BulletinoftheKoreanChemicalSociety,2019,vol.40,p.146-149

[33]JournaloftheAmericanChemicalSociety,2019

108-24-7    60646-30-2   
(S)-1-(9-anthryl)-2,2,2-trifluoroethylacetate 

[1]BulletinoftheChemicalSocietyofJapan,1996,vol.69,p.1755-1761

60646-30-2   
di(S)-1-(9-anthryl)-2,2,2-trifluoroethylsulphite 

[1]TetrahedronAsymmetry,2001,vol.12,p.1737-1740

Literature fold

Title: Chemical profiling of the cytotoxic triterpenoid-concentrating fraction and characterization of ergostane stereo-isomer ingredients from Antrodia camphorata.

Journal: Journal of pharmaceutical and biomedical analysis20120125

Title: Phosphorus-nitrogen compounds. 21. Syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclic phosphazene derivatives. The NMR behaviors of chiral phosphazenes with stereogenic centers upon the addition of chiral solvating agents.

Journal: Inorganic chemistry20100802

Title: Phosphorus-nitrogen compounds. 18. Syntheses, stereogenic properties, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic mono- and bisferrocenylphosphazene derivatives.

Journal: Inorganic chemistry20091102

Title: The structural and stereogenic properties of pentaerythritoxy-bridged cyclotriphosphazene derivatives: spiro-spiro, spiro-ansa and ansa-ansa isomers.

Journal: Dalton transactions (Cambridge, England : 2003)20060314

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