Home Other Building Blocks 1006-64-0
1006-64-0,MFCD01631835
Catalog No.:AA0002D2

1006-64-0 | 2-Phenylpyrrolidine

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1g
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$24.00   $17.00
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5g
97%
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$38.00   $27.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0002D2
Chemical Name:
2-Phenylpyrrolidine
CAS Number:
1006-64-0
Molecular Formula:
C10H13N
Molecular Weight:
147.2169
MDL Number:
MFCD01631835
SMILES:
C1CNC(C1)c1ccccc1
NSC Number:
94961
Properties
Properties
 
BP:
237°C at 760 mmHg  
Form:
Liquid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
116  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
1.8  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2006,vol.128,p.2224-2225

[2]TetrahedronLetters,1997,vol.38,p.7487-7490

[3]Patent:US5292893,1994,A

[4]JournalofOrganicChemistry,1997,vol.62,p.7726-7735

[5]Chemistry-AEuropeanJournal,2019,vol.25,p.1918-1922

[6]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1957,vol.77,p.1062    Chem.Abstr.,1958,p.5376

[7]JournalofOrganicChemistry,1980,vol.45,p.2489-2498

[8]BioorganicandMedicinalChemistry,2001,vol.9,p.2105-2111

[9]JournalofCatalysis,2004,vol.224,p.170-177

[10]JournaloftheAmericanChemicalSociety,2002,vol.124,p.3220-3221

[11]AdvancedSynthesisandCatalysis,2004,vol.346,p.1316-1328

[12]Patent:WO2005/56513,2005,A1.Locationinpatent:Page/Pagecolumn30

[13]Patent:WO2005/56513,2005,A1.Locationinpatent:Page/Pagecolumn30

[14]Patent:WO2005/56513,2005,A1.Locationinpatent:Page/Pagecolumn30

[15]Patent:WO2005/56513,2005,A1.Locationinpatent:Page/Pagecolumn30

[16]AngewandteChemie-InternationalEdition,2018,vol.57,p.1863-1868    Angew.Chem.,2018,vol.130,p.1881-1886,6

[17]Tetrahedron,2018,vol.74,p.3947-3954

[18]JournaloftheAmericanChemicalSociety,2018,vol.140,p.13171-13175

[19]JournaloftheAmericanChemicalSociety,2019,vol.141,p.15869-15878

[20]Bioorganicandmedicinalchemistryletters,2020,vol.30

[1]JournalofMedicinalChemistry,1984,vol.27,p.943-946

[2]JournalofMedicinalChemistry,1987,vol.30,p.1433-1454

[1]TetrahedronLetters,1984,vol.25,p.5271-5274

[1]JournalofOrganicChemistry,1992,vol.57,p.1656-1662

[1]JournalofOrganicChemistry,1991,vol.56,p.2294-2296

Literature

Title: Highly effective asymmetric hydrogenation of cyclic N-alkyl imines with chiral cationic Ru-MsDPEN catalysts.

Journal: Organic letters 20110819

Title: [Regioselectivity in the dehydrogenation of substituted ethylenediamines as nicotine models].

Journal: Die Pharmazie 20090901

Title: A spectroscopic study of nicotine analogue 2-phenylpyrrolidine (PPD) using resonant two-photon ionization (R2PI), microwave, and 2D NMR techniques.

Journal: Journal of the American Chemical Society 20090225

Title: Determination of the natural abundance delta15N of nicotine and related alkaloids by gas chromatography/isotope ratio mass spectrometry.

Journal: Rapid communications in mass spectrometry : RCM 20050101

Title: 1,2,5-Substituted derivatives of 2-phenylpyrrolidine.

Journal: Acta crystallographica. Section C, Crystal structure communications 20040601

Title: Asymmetric alkyldifluoroboranes and their use in secondary amine synthesis.

Journal: Organic letters 20020627

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