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63012-03-3,MFCD06201252
Catalog No.:AA00E99R

63012-03-3 | 3-Chlorobenzhydrol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$6.00   $4.00
- +
1g
95%
in stock  
$11.00   $8.00
- +
25g
95%
in stock  
$95.00   $67.00
- +
  • 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:
AA00E99R
Chemical Name:
3-Chlorobenzhydrol
CAS Number:
63012-03-3
Molecular Formula:
C13H11ClO
Molecular Weight:
218.6788
MDL Number:
MFCD06201252
SMILES:
Clc1cccc(c1)C(c1ccccc1)O
Properties
Properties
 
BP:
342.6°C at 760 mmHg  
Form:
Liquid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
189  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
3.8  

Upstream Synthesis Route

[1]OrganicLetters,2000,vol.2,#5,p.659-661

[2]Patent:EP1437344,2004,A1,.Locationinpatent:Page48

[3]RecueildesTravauxChimiquesdesPays-Bas,1912,vol.31,p.311

[4]RecueildesTravauxChimiquesdesPays-Bas,1915,vol.34,p.162

[5]RecueildesTravauxChimiquesdesPays-Bas,1919,vol.38,p.121

[6]JournaloftheChemicalSociety,1940,p.1011,1014

[7]JournaloftheAmericanChemicalSociety,1955,vol.77,p.4007,4008

[8]JournalofOrganicChemistry,1967,vol.32,p.2692-2695

[9]Tetrahedron:Asymmetry,1991,vol.2,#5,p.339-342

[10]BulletindelaSocieteChimiquedeFrance,1994,vol.131,#6,p.632-635

[11]BioorganicandMedicinalChemistryLetters,1996,vol.6,#3,p.311-314

[12]JournalofMedicinalChemistry,1997,vol.40,#6,p.851-857

[13]JournalofPhysicalOrganicChemistry,1998,vol.11,#3,p.223-229

[14]Chemistry-AEuropeanJournal,2006,vol.12,#6,p.1648-1656

[15]ArchivderPharmazie,2011,vol.344,#6,p.402-410

[16]Tetrahedron,2019,vol.75,#2,p.308-314

[1]TetrahedronLetters,2011,vol.52,#14,p.1677-1679

[1]TetrahedronLetters,2013,vol.54,#13,p.1747-1750

[2]Patent:US5719168,1998,A,

[1]TetrahedronLetters,2010,vol.51,#6,p.924-927

[1]AngewandteChemie,1981,vol.93,#3,p.287-288

[2]ChemischeBerichte,1985,vol.118,#9,p.3872-3899

Downstream Synthesis Route

[1]OrganicLetters,2000,vol.2,p.659-661

[2]Patent:EP1437344,2004,A1.Locationinpatent:Page48

[3]RecueildesTravauxChimiquesdesPays-Bas,1912,vol.31,p.311

[4]RecueildesTravauxChimiquesdesPays-Bas,1915,vol.34,p.162

[5]RecueildesTravauxChimiquesdesPays-Bas,1919,vol.38,p.121

[6]JournaloftheChemicalSociety,1940,p.1011,1014

[7]JournaloftheAmericanChemicalSociety,1955,vol.77,p.4007,4008

[8]JournalofOrganicChemistry,1967,vol.32,p.2692-2695

[9]TetrahedronAsymmetry,1991,vol.2,p.339-342

[10]BulletindelaSocieteChimiquedeFrance,1994,vol.131,p.632-635

[11]BioorganicandMedicinalChemistryLetters,1996,vol.6,p.311-314

[12]JournalofMedicinalChemistry,1997,vol.40,p.851-857

[13]JournalofPhysicalOrganicChemistry,1998,vol.11,p.223-229

[14]Chemistry-AEuropeanJournal,2006,vol.12,p.1648-1656

[15]ArchivderPharmazie,2011,vol.344,p.402-410

[16]Tetrahedron,2019,vol.75,p.308-314

[1]Chemistry-AEuropeanJournal,2006,vol.12,p.1648-1656

[2]JournaloftheAmericanChemicalSociety,1928,vol.50,p.1811

[3]JournalofOrganicChemistry,1967,vol.32,p.2692-2695

[4]JournalofMedicinalChemistry,1997,vol.40,p.851-857

[5]JournalofPhysicalOrganicChemistry,1998,vol.11,p.223-229

[6]BioorganicandMedicinalChemistryLetters,2010,vol.20,p.1378-1383

[7]ArchivderPharmazie,2011,vol.344,p.402-410

phenylmagnesiumbromide 
  587-04-2    63012-03-3 

[1]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1925,vol.56,p.150    ChemischesZentralblatt,1926,vol.97,p.919

[1]Diss.<Univ.Berlin1933>S.31,35,

[1]Chemistry-AEuropeanJournal,2006,vol.12,p.1648-1656

[2]CollectionofCzechoslovakChemicalCommunications,1972,vol.37,p.2568-2578

Literature
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SDS
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