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1561-86-0,MFCD00003860
Catalog No.:AA001OFO

1561-86-0 | 2-Chlorocyclohexanol

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1g
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$18.00   $13.00
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5g
95%
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$70.00   $49.00
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25g
95%
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$133.00   $93.00
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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:
AA001OFO
Chemical Name:
2-Chlorocyclohexanol
CAS Number:
1561-86-0
Molecular Formula:
C6H11ClO
Molecular Weight:
134.6039
MDL Number:
MFCD00003860
SMILES:
OC1CCCCC1Cl
Properties
Properties
 
BP:
218.3°C at 760 mmHg  
Form:
Liquid  
MP:
29℃  
Refractive Index:
n20/D 1.488(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
74.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Undefined Atom Stereocenter Count:
3  
XLogP3:
1.5  

Downstream Synthesis Route
1561-86-0    13697-91-1   
hexahydro-spirobenzofuran-3,1'-cyclopentane-2,2'-dione 

[1]Winternitz;Thakkar[BulletindelaSocieteChimiquedeFrance,1952,p.471,475]

[1]Godchot[ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1923,vol.176,p.449]

[2]OrangicSyntheses[CollectiveVol.I<NewYork1932>,S.179]

[3]Detoeuf[BulletindelaSocieteChimiquedeFrance,1922,vol.<4>31,p.178]

[4]Koopmeiners,Julia;Diederich,Christina;Solarczek,Jennifer;Voß,Hauke;Mayer,Janine;Blankenfeldt,Wulf;Schallmey,Anett[ACSCatalysis,2017,vol.7,#10,p.6877-6886]

854435-42-0    1561-86-0   
sulfurousacidbis-(2-chloro-cyclohexylester) 

[1]Bloomfield[JournaloftheChemicalSociety,1944,p.114,119]

[1]Koetz;Merkel[JournalfurpraktischeChemie(Leipzig1954),1926,vol.<2>113,p.74]

[1]Detoeuf[BulletindelaSocieteChimiquedeFrance,1922,vol.<4>31,p.178]

Literature

Title: Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

Journal: Journal of analytical methods in chemistry 20120101

Title: Enantioseparation of chiral alcohols by complex formation and subsequent supercritical fluid extraction.

Journal: Chirality 20031101

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SDS
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