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1,3-Cyclohexanediol

  • CAS: 504-01-8
  • Purity: 99%
  • Reputable manufacturer supply 1,3-Cyclohexanediol 504-01-8 in stock with high standard
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Reputable manufacturer supply 1,3-Cyclohexanediol 504-01-8 in stock with high standard

  • Molecular Formula: C6H12O2
  • Molecular Weight: 116.16
  • Appearance/Colour: clear slightly yellow viscous liquid after melting 
  • Vapor Pressure: 0.00445mmHg at 25°C 
  • Melting Point: 30 °C 
  • Refractive Index: 1.495-1.497  
  • Boiling Point: 246.5 °C at 760 mmHg 
  • PKA: 14.70±0.40(Predicted) 
  • Flash Point: 123.9 °C 
  • PSA: 40.46000 
  • Density: 1.156 g/cm3 
  • LogP: 0.28220 

1,3-Cyclohexanediol(Cas 504-01-8) Usage

InChI:InChI=1/C6H12O2/c7-5-2-1-3-6(8)4-5/h5-8H,1-4H2/t5-,6-/m1/s1

504-01-8 Relevant articles

Selective hydrogenation of lignin-derived compounds under mild conditions

Chen, Lu,Van Muyden, Antoine P.,Cui, Xinjiang,Laurenczy, Gabor,Dyson, Paul J.

, p. 3069 - 3073 (2020/06/17)

A key challenge in the production of lig...

A stable and practical nickel catalyst for the hydrogenolysis of C-O bonds

Cui, Xinjiang,Yuan, Hangkong,Junge, Kathrin,Topf, Christoph,Beller, Matthias,Shi, Feng

, p. 305 - 310 (2017/01/24)

The selective hydrogenolysis of C-O bond...

Upgrading of aromatic compounds in bio-oil over ultrathin graphene encapsulated Ru nanoparticles

Shi, Juanjuan,Zhao, Mengsi,Wang, Yingyu,Fu, Jie,Lu, Xiuyang,Hou, Zhaoyin

supporting information, p. 5842 - 5848 (2016/05/24)

Fast pyrolysis of biomass for bio-oil pr...

Ruthenium Nanoparticles Stabilized in Cross-Linked Dendrimer Matrices: Hydrogenation of Phenols in Aqueous Media

Maximov, Anton,Zolotukhina, Anna,Murzin, Vadim,Karakhanov, Edward,Rosenberg, Edward

, p. 1197 - 1210 (2015/04/14)

Novel catalysts consisting of ruthenium ...

504-01-8 Process route

cyclohexane
110-82-7,25012-93-5

cyclohexane

cyclohexyl hydroperoxide
766-07-4

cyclohexyl hydroperoxide

cyclohexane-1,3-diol
504-01-8

cyclohexane-1,3-diol

4-hydroxycyclohexanone
13482-22-9

4-hydroxycyclohexanone

2,4-dihydroxycyclohexanone
1452767-32-6

2,4-dihydroxycyclohexanone

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

cyclohexanone-2-ol
533-60-8

cyclohexanone-2-ol

1,4-Cyclohexanedione
637-88-7

1,4-Cyclohexanedione

Conditions
Conditions Yield
With 2-pyrazylcarboxylic acid; dihydrogen peroxide; In acetonitrile; at 60 ℃; for 24h;
cyclohexane
110-82-7,25012-93-5

cyclohexane

cyclohexyl hydroperoxide
766-07-4

cyclohexyl hydroperoxide

cyclohexane-1,3-diol
504-01-8

cyclohexane-1,3-diol

4-hydroxycyclohexanone
13482-22-9

4-hydroxycyclohexanone

2,4-dihydroxycyclohexanone
1452767-32-6

2,4-dihydroxycyclohexanone

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

cyclohexanone-2-ol
533-60-8

cyclohexanone-2-ol

1,4-Cyclohexanedione
637-88-7

1,4-Cyclohexanedione

cyclohexanol
108-93-0

cyclohexanol

Conditions
Conditions Yield
With 2-pyrazylcarboxylic acid; dihydrogen peroxide; In acetonitrile; at 60 ℃; for 24h; Reagent/catalyst; Temperature; Time; Concentration;

504-01-8 Upstream products

  • 5515-64-0
    5515-64-0

    trans-1,3-cyclohexanediol

  • 504-02-9
    504-02-9

    1,3-cylohexanedione

  • 108-46-3
    108-46-3

    recorcinol

  • 108-94-1
    108-94-1

    cyclohexanone

504-01-8 Downstream products

  • 812682-36-3
    812682-36-3

    1,3-bis-chloromethoxy-cyclohexane

  • 16327-00-7
    16327-00-7

    3-methoxycyclohexan-1-ol

  • 36897-97-9
    36897-97-9

    1,3-dimethoxy-cyclohexane

  • 823-19-8
    823-19-8

    3-hydroxycyclohexanone

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