Synthesis
ChemicalBook > CAS DataBase List > cis-1,2-Cyclohexanediol

cis-1,2-Cyclohexanediol

Synthesis
Product Name
cis-1,2-Cyclohexanediol
CAS No.
1792-81-0
Chemical Name
cis-1,2-Cyclohexanediol
Synonyms
Grandidentol;TIMTEC-BB SBB007678;CIS-HEXAHYDROCATECHOL;CIS-1,2-CYCLOHEXANEDIOL;1,2-cis-cyclohexanediol;Adipic Acid Impurity 29;cis-Cyclohexane-1,2-diol;cis-2-Hydroxycyclohexanol;1,2-Cyclohexanediol, cis-;(1S)-1α,2α-Cyclohexanediol
CBNumber
CB8159715
Molecular Formula
C6H12O2
Formula Weight
116.16
MOL File
1792-81-0.mol
More
Less

cis-1,2-Cyclohexanediol Property

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)
More
Less

Safety

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

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
361267
Product name
cis-1,2-Cyclohexanediol
Purity
99%
Packaging
1g
Price
$56.3
Updated
2024/03/01
TCI Chemical
Product number
C1802
Product name
cis-1,2-Cyclohexanediol
Purity
>98.0%(GC)
Packaging
1g
Price
$51
Updated
2024/03/01
TRC
Product number
C997755
Product name
cis-1,2-Cyclohexanediol
Packaging
250mg
Price
$85
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC58748
Product name
cis-1,2-Cyclohexanediol
Packaging
1g
Price
$90
Updated
2021/12/16
AK Scientific
Product number
M185
Product name
cis-1,2-Cyclohexanediol
Packaging
1g
Price
$94
Updated
2021/12/16
More
Less

cis-1,2-Cyclohexanediol Chemical Properties,Usage,Production

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.

cis-1,2-Cyclohexanediol Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

cis-1,2-Cyclohexanediol Suppliers

Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38631
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Frinton Laboratories Inc.,
Tel
--
Fax
--
Country
United States
ProdList
355
Advantage
58
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
CarboMer, Inc.
Tel
--
Fax
--
Email
sales@carbomer.com
Country
United States
ProdList
4026
Advantage
67
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Frinton Laboratories, Inc.
Tel
--
Fax
--
Email
sales@frinton.com
Country
United States
ProdList
1459
Advantage
61
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
Crescent Chemical Co., Inc.
Tel
--
Fax
--
Email
sales@creschem.com
Country
United States
ProdList
4597
Advantage
68
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
TimTec Corporation
Tel
--
Fax
--
Email
info@timtec.net
Country
United States
ProdList
6891
Advantage
68
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
ASDI Incorporated
Tel
--
Fax
--
Email
customerservice@asdi.net
Country
United States
ProdList
6922
Advantage
67
Eastar Chemical Corporation
Tel
--
Fax
--
Email
info@eastarchem.com
Country
United States
ProdList
129
Advantage
38

1792-81-0, cis-1,2-CyclohexanediolRelated Search:


  • 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
  • cis-Cyclohexane-1,2-diol
  • cis-1,2-Cyclohexanediol 99%
  • <i>cis</i>-1,2-Cyclohexanediol
  • TIMTEC-BB SBB007678
  • 1,2-Cyclohexanediol, cis-
  • Grandidentol
  • CIS-HEXAHYDROBRENZCATECHIN
  • CIS-HEXAHYDROCATECHOL
  • CIS-1,2-CYCLOHEXANEDIOL
  • CIS-1,2-DIHYDROXYCYCLOHEXANE
  • (1R,2S)-cyclohexane-1,2-diol
  • 1,2-cis-Dihydroxycyclohexane
  • cis-hexahydrobrenzkatechin
  • rel-((1R,2S)-Cyclohexane-1,2-diol)
  • cis-1,2-Cyclohexanediol &gt
  • 1,2-Cyclohexanediol, (1R,2S)-rel-
  • 1,2-cis-cyclohexanediol
  • Adipic Acid Impurity 29
  • 1792-81-0
  • 1972-81-0
  • Organic Building Blocks
  • Oxygen Compounds
  • Polyols
  • Building Blocks
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Aromatic alcohols and diols
  • Organic Building Blocks
  • Oxygen Compounds
  • Polyols