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cis-1,2-Cyclohexanediol

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cis-1,2-Cyclohexanediol Basic information

Product Name:
cis-1,2-Cyclohexanediol
Synonyms:
  • 1,2-Cyclohexanediol, (1R,2S)-
  • cis-2-Hydroxycyclohexanol
  • meso-cis-1,2-Cyclohexanediol
  • (1R,2S)-1,2-Cyclohexanediol
  • (1S)-1α,2α-Cyclohexanediol
  • (1α,2α)-1,2-Cyclohexanediol
  • cis-1,2-Cyclohexanediol,99%
  • cis-1,2-Cyclohexanediol, 99% 1GR
CAS:
1792-81-0
MF:
C6H12O2
MW:
116.16
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Aromatic alcohols and diols
  • Organic Building Blocks
  • Organic Building Blocks
  • Oxygen Compounds
  • Oxygen Compounds
  • Polyols
Mol File:
1792-81-0.mol
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cis-1,2-Cyclohexanediol Chemical Properties

Melting point:
97-101 °C (lit.)
Boiling point:
116 °C / 13mmHg
Density 
1.0297
refractive index 
1.4270 (estimate)
solubility 
soluble in Methanol
form 
Crystalline Flakes or Powder
pka
14.49±0.40(Predicted)
color 
White to light beige
Water Solubility 
slightly soluble
BRN 
1340578
CAS DataBase Reference
1792-81-0(CAS DataBase Reference)
NIST Chemistry Reference
cis-1,2-Cyclohexanediol(1792-81-0)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
3-10
HS Code 
29061990

MSDS

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cis-1,2-Cyclohexanediol Usage And Synthesis

Synthesis

To a mixture of N-methylmorpholine-N-oxide.2H2O (18.2 g, 155 mmol), water  (50 mL), acetone (20 mL), and osmium tetroxide (80 mg) in t-butanol (8 mL) was added distilled cyclohexene (10.1 mL, 100 mmol). The reaction was slightly exothermic initially and was maintained at room temperature with a water bath. The reaction was complete after stirring overnight at room temperature under nitrogen. A slurry of 1 g of sodium hydrosulfifite, 12 g of magnesium silicate (magnesol), and 80 ml of water was added, and the magnesol was fifiltered. The fifiltrate was neutralized to pH 7 with 1 N H2SO4, the acetone was evaporated under vacuum, and the pH was further adjusted to pH 2. The solution was saturated with NaCl and extracted with EtOAc. The aqueous phase was concentrated by azeotroping with n-butanol and further extracted with ethyl acetate. The combined ethyl acetate layers were dried and evaporated, yielding 11.2 g (96.6%) of crystalline solid. Recrystallization from ether provided 10.6 g (91%) of cis-1,2-cyclohexanediol, mp 95–97°C.

Reference: Van Rheenen, V.; Kelly, R. C.; Cha, D. Y. Tetrahedron Lett. 1976, 17, 1973−1976.

Chemical Properties

White to light beige crystalline flakes or powder

Uses

cis-1,2-Cyclohexanediol is a reagent used in the synthesis of boronic esters of corannulene which are used to prepare icosahedral supramolecules.

Definition

ChEBI: A cyclohexane-1,2-diol with cis-configuration.

General Description

Core-shell-like silica nickel species nanoparticle catalyzed dehydrogenation of 1,2-cyclohexanediol to catechol is reported. Crystal structure of a Cr(V) complex with cis-1,2-cyclohexanediol is reported. Enzymatic oxidation of cis-1,2-cyclohexanediol by Gluconobacter oxydans (ATCC 621) is reported.

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