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1792-81-0,MFCD00064944
Catalog No.:AA0026SD

1792-81-0 | Cis-1,2-cyclohexanediol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$34.00   $24.00
- +
1g
>98.0%(GC)
in stock  
$59.00   $41.00
- +
5g
98%
in stock  
$146.00   $102.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0026SD
Chemical Name:
Cis-1,2-cyclohexanediol
CAS Number:
1792-81-0
Molecular Formula:
C6H12O2
Molecular Weight:
116.1583
MDL Number:
MFCD00064944
SMILES:
O[C@@H]1CCCC[C@@H]1O
Properties
Properties
 
BP:
116°C at 13 mmHg  
Form:
Solid  
MP:
97-101 °C(lit.);  
Refractive Index:
1.4270 (estimate)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
62.9  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.2  

Downstream Synthesis Route

[1]Hao,Bo;Gunaratna,MedhaJ.;Zhang,Man;Weerasekara,Sahani;Seiwald,SarahN.;Nguyen,VuT.;Meier,Alex;Hua,DuyH.[JournaloftheAmericanChemicalSociety,2016,vol.138,#51,p.16839-16848]

[2]Posternaketal.[HelveticaChimicaActa,1955,vol.38,p.205,209]

[1]Mueller,ChristianE.;Hrdina,Radim;Wende,RaffaelC.;Schreiner,PeterR.[Chemistry-AEuropeanJournal,2011,vol.17,#23,p.6309-6314]

[2]Winsteinetal.[JournaloftheAmericanChemicalSociety,1948,vol.70,p.816,818]

[3]Winstein;Buckles[JournaloftheAmericanChemicalSociety,1942,vol.64,p.2780,2784]

[4]Clarke,PaulA.;Kayaleh,NadimE.;Smith,MartinA.;Baker,JamesR.;Bird,StephanJ.;Chan,Chuen[JournalofOrganicChemistry,2002,vol.67,#15,p.5226-5231]

[1]Wolfe,MichaelS.[SyntheticCommunications,1997,vol.27,#17,p.2975-2984]

[2]Sano;Ohashi;Oriyama[Synthesis,1999,#7,p.1141-1144]

[3]Wang,Yaxin;Hu,Xiafei;Morales-Rivera,CristianA.;Li,Guo-Xing;Huang,Xin;He,Gang;Liu,Peng;Chen,Gong[JournaloftheAmericanChemicalSociety,2018,vol.140,#30,p.9678-9684]

[4]Verkadeetal.[JustusLiebigsAnnalenderChemie,1930,vol.477,p.279,288]Lindemann;deLange[JustusLiebigsAnnalenderChemie,1930,vol.483,p.31,39]Rothstein[AnnalesdeChimie(Cachan,France),1930,vol.<10>14,p.461,515]

[5]Brunel[AnnalesdeChimie(Cachan,France),1905,vol.<8>6,p.208][BulletindelaSocieteChimiquedeFrance,1905,vol.<3>33,p.269]Brunel[ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1903,vol.136,p.384][BulletindelaSocieteChimiquedeFrance,1903,vol.<3>29,p.233]

[6]Macias-Ruvalcaba,NormaA.;Moy,CherylL.;Zheng,Zi-Rong;Evans,DennisH.[JournalofOrganicChemistry,2006,vol.71,#13,p.4829-4834]

[1]Covert;Connor;Adkins[JournaloftheAmericanChemicalSociety,1932,vol.54,p.1651,1658]Amatatsu[NipponKagakuKaishi/JournaloftheChemicalSocietyofJapan,1931,vol.52,p.585,587][Chem.Abstr.,1932,p.5084]

[2]Palfray[BulletindelaSocieteChimiquedeFrance,1940,vol.<5>7,p.440][JournaloftheAmericanChemicalSociety,1941,vol.63,p.3541]English;Barber[JournaloftheAmericanChemicalSociety,1949,vol.71,p.3310]

[1]Houk,J.;Whitesides,G.M.[JournaloftheAmericanChemicalSociety,1987,vol.109,p.6825]

[2]Criegee;Stanger[ChemischeBerichte,1936,vol.69,p.2753,2755]

[3]Rebrovic,Louis;Koser,GeraldF.[JournalofOrganicChemistry,1984,vol.49,#13,p.2462-2472]

Literature

Title: Assessment of the nuclear pore dilating agent trans-cyclohexane-1,2-diol in differentiated airway epithelium.

Journal: The journal of gene medicine 20120701

Title: Theoretical study of oxidation of cyclohexane diol to adipic anhydride by [Ru(IV)(O)(tpa)(H2O)]2+ complex (tpa ═ tris(2-pyridylmethyl)amine).

Journal: Inorganic chemistry 20110704

Title: A very active cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides.

Journal: The Journal of organic chemistry 20100604

Title: On the origins of kinetic resolution of cyclohexane-1,2-diols through stereoselective acylation by chiral tetrapeptides.

Journal: Organic letters 20090806

Title: From simple diols to carbohydrate derivatives of phenylarsonic acid.

Journal: Inorganic chemistry 20090202

Title: Oxidation of cyclohexanediol derivatives with 12-tungstophosphoric acid-hydrogen peroxide system.

Journal: Journal of oleo science 20090101

Title: Advantages of synthesizing trans-1,2-cyclohexanediol in a continuous flow microreactor over a standard glass apparatus.

Journal: The Journal of organic chemistry 20071221

Title: Biocatalytic production of enantiopure cyclohexane-trans-1,2-diol using extracellular lipases from Bacillus subtilis.

Journal: Applied microbiology and biotechnology 20061001

Title: Absence of interactive effects of trans-1,2-cyclohexanediol, a major metabolite of the side-chain of candesartan cilexetil, on digoxin-induced arrhythmias in dogs.

Journal: Journal of pharmacological sciences 20030801

Title: Tin(II) chloride catalyzed reactions of diazodiphenylmethane with vicinal diols in an aprotic solvent. The reactions with cis- and trans-1,2-cyclohexanediols and 1,2-propanediol.

Journal: Carbohydrate research 20030422

Title: Expression of benzene dioxygenase from Pseudomonas putida ML2 in cis-1,2-cyclohexanediol-degrading pseudomonads.

Journal: Applied microbiology and biotechnology 20010601

Title: Asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids using (S,S)-cyclohexane-1,2-diol as a chiral auxiliary.

Journal: The Journal of organic chemistry 20010420

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Tags:1792-81-0 Molecular Formula|1792-81-0 MDL|1792-81-0 SMILES|1792-81-0 Cis-1,2-cyclohexanediol
Catalog No.: AA0026SD
1792-81-0,MFCD00064944
1792-81-0 | Cis-1,2-cyclohexanediol
Pack Size： 250mg
Purity： 95%
in stock
$34.00 $24.00
Pack Size： 1g
Purity： >98.0%(GC)
in stock
$59.00 $41.00
Pack Size： 5g
Purity： 98%
in stock
$146.00 $102.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0026SD
Chemical Name: Cis-1,2-cyclohexanediol
CAS Number: 1792-81-0
Molecular Formula: C6H12O2
Molecular Weight: 116.1583
MDL Number: MFCD00064944
SMILES: O[C@@H]1CCCC[C@@H]1O
Properties
BP: 116°C at 13 mmHg  
Form: Solid  
MP: 97-101 °C(lit.);  
Refractive Index: 1.4270 (estimate)  
Storage: Keep in dry area;2-8℃;  
Complexity: 62.9  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.2  
Downstream Synthesis Route
1792-81-0    53439-93-3 

[1]Hao,Bo;Gunaratna,MedhaJ.;Zhang,Man;Weerasekara,Sahani;Seiwald,SarahN.;Nguyen,VuT.;Meier,Alex;Hua,DuyH.[JournaloftheAmericanChemicalSociety,2016,vol.138,#51,p.16839-16848]

[2]Posternaketal.[HelveticaChimicaActa,1955,vol.38,p.205,209]

1792-81-0    108-24-7    2396-76-1    86703-56-2 

[1]Mueller,ChristianE.;Hrdina,Radim;Wende,RaffaelC.;Schreiner,PeterR.[Chemistry-AEuropeanJournal,2011,vol.17,#23,p.6309-6314]

[2]Winsteinetal.[JournaloftheAmericanChemicalSociety,1948,vol.70,p.816,818]

[3]Winstein;Buckles[JournaloftheAmericanChemicalSociety,1942,vol.64,p.2780,2784]

[4]Clarke,PaulA.;Kayaleh,NadimE.;Smith,MartinA.;Baker,JamesR.;Bird,StephanJ.;Chan,Chuen[JournalofOrganicChemistry,2002,vol.67,#15,p.5226-5231]

1792-81-0    98-88-4    37854-29-8 

[1]Wolfe,MichaelS.[SyntheticCommunications,1997,vol.27,#17,p.2975-2984]

[2]Sano;Ohashi;Oriyama[Synthesis,1999,#7,p.1141-1144]

[3]Wang,Yaxin;Hu,Xiafei;Morales-Rivera,CristianA.;Li,Guo-Xing;Huang,Xin;He,Gang;Liu,Peng;Chen,Gong[JournaloftheAmericanChemicalSociety,2018,vol.140,#30,p.9678-9684]

[4]Verkadeetal.[JustusLiebigsAnnalenderChemie,1930,vol.477,p.279,288]Lindemann;deLange[JustusLiebigsAnnalenderChemie,1930,vol.483,p.31,39]Rothstein[AnnalesdeChimie(Cachan,France),1930,vol.<10>14,p.461,515]

[5]Brunel[AnnalesdeChimie(Cachan,France),1905,vol.<8>6,p.208][BulletindelaSocieteChimiquedeFrance,1905,vol.<3>33,p.269]Brunel[ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1903,vol.136,p.384][BulletindelaSocieteChimiquedeFrance,1903,vol.<3>29,p.233]

[6]Macias-Ruvalcaba,NormaA.;Moy,CherylL.;Zheng,Zi-Rong;Evans,DennisH.[JournalofOrganicChemistry,2006,vol.71,#13,p.4829-4834]

120-80-9    1792-81-0    931-17-9 

[1]Covert;Connor;Adkins[JournaloftheAmericanChemicalSociety,1932,vol.54,p.1651,1658]Amatatsu[NipponKagakuKaishi/JournaloftheChemicalSocietyofJapan,1931,vol.52,p.585,587][Chem.Abstr.,1932,p.5084]

[2]Palfray[BulletindelaSocieteChimiquedeFrance,1940,vol.<5>7,p.440][JournaloftheAmericanChemicalSociety,1941,vol.63,p.3541]English;Barber[JournaloftheAmericanChemicalSociety,1949,vol.71,p.3310]

1792-81-0    98-59-9    5433-22-7 

[1]Houk,J.;Whitesides,G.M.[JournaloftheAmericanChemicalSociety,1987,vol.109,p.6825]

[2]Criegee;Stanger[ChemischeBerichte,1936,vol.69,p.2753,2755]

[3]Rebrovic,Louis;Koser,GeraldF.[JournalofOrganicChemistry,1984,vol.49,#13,p.2462-2472]

Literature fold

Title: Assessment of the nuclear pore dilating agent trans-cyclohexane-1,2-diol in differentiated airway epithelium.

Journal: The journal of gene medicine20120701

Title: Theoretical study of oxidation of cyclohexane diol to adipic anhydride by [Ru(IV)(O)(tpa)(H2O)]2+ complex (tpa ═ tris(2-pyridylmethyl)amine).

Journal: Inorganic chemistry20110704

Title: A very active cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides.

Journal: The Journal of organic chemistry20100604

Title: On the origins of kinetic resolution of cyclohexane-1,2-diols through stereoselective acylation by chiral tetrapeptides.

Journal: Organic letters20090806

Title: From simple diols to carbohydrate derivatives of phenylarsonic acid.

Journal: Inorganic chemistry20090202

Title: Oxidation of cyclohexanediol derivatives with 12-tungstophosphoric acid-hydrogen peroxide system.

Journal: Journal of oleo science20090101

Title: Advantages of synthesizing trans-1,2-cyclohexanediol in a continuous flow microreactor over a standard glass apparatus.

Journal: The Journal of organic chemistry20071221

Title: Biocatalytic production of enantiopure cyclohexane-trans-1,2-diol using extracellular lipases from Bacillus subtilis.

Journal: Applied microbiology and biotechnology20061001

Title: Absence of interactive effects of trans-1,2-cyclohexanediol, a major metabolite of the side-chain of candesartan cilexetil, on digoxin-induced arrhythmias in dogs.

Journal: Journal of pharmacological sciences20030801

Title: Tin(II) chloride catalyzed reactions of diazodiphenylmethane with vicinal diols in an aprotic solvent. The reactions with cis- and trans-1,2-cyclohexanediols and 1,2-propanediol.

Journal: Carbohydrate research20030422

Title: Expression of benzene dioxygenase from Pseudomonas putida ML2 in cis-1,2-cyclohexanediol-degrading pseudomonads.

Journal: Applied microbiology and biotechnology20010601

Title: Asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids using (S,S)-cyclohexane-1,2-diol as a chiral auxiliary.

Journal: The Journal of organic chemistry20010420

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