1,2-Cyclohexanediol
Product Information
Molecular Formula
C6H12O2
Molecular Weight
116.16
Description
Cyclohexane-1,2-diol is a diol that consists of a cyclohexane skeleton carrying two hydroxy substituents.
Synonyms
1,2-Benzenediol, hexahydro-; 1,2-Cyclohexanediol cis-trans; 1,2-cyclohexanediol(cis-andtrans-mixture; 1,2-Cyclohexanediol,c&t; 1,2-cyclohexanediol,mixtureofcisandtrans; 2-Hydroxycyclohexanol; Brenzcatechin; Brenzkatechin
IUPAC Name
cyclohexane-1,2-diol
SMILES
C1CCC(C(C1)O)O
InChI
InChI=1S/C6H12O2/c7-5-3-1-2-4-6(5)8/h5-8H,1-4H2
InChI Key
PFURGBBHAOXLIO-UHFFFAOYSA-N
Boiling Point
118-120°C (10 mmHg)
Melting Point
73-77°C
Purity
95%
Density
1.156 g/cm3
Appearance
beige crystals.
Computed Properties
XLogP3
0.2
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
116.083729621 g/mol
Monoisotopic Mass
116.083729621 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
62.9
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
2
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114181784-A | Composition for cleaning blue-light-proof resin lens and preparation method and application thereof | 2021-12-09 |
| CN-114058003-A | Double metal cyanide catalyst convenient to separate and preparation method thereof | 2021-12-06 |
| CN-114085370-A | Poly (carbonate-ether) polyol dispersant, high-stability polymer polyol and preparation method thereof | 2021-12-06 |
| CN-113952948-A | Molybdenum oxide catalyst for preparing cyclohexanediol by oxidizing cyclohexene and preparation method and application thereof | 2021-11-19 |
| CN-113980252-A | Continuous production method of modified poly (butylene succinate) | 2021-11-19 |
| CN-113773418-A | Polystyrene selenizing method using diselenide as selenium source | 2021-10-22 |
| CN-113980259-A | Method for preparing polycarbonate by using 1,1,3,3,4,4,6, 6-octamethyltetrahydropentene-2, 5-diol | 2021-10-14 |
| CN-113943217-A | Method for recovering dipolyketone in cyclohexane oxidation by-product X oil | 2021-08-31 |
| JP-6994600-B1 | Primer composition | 2021-08-31 |
| JP-6994601-B1 | Primer composition | 2021-08-31 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22711445 | 2012-07-01 | Assessment of the nuclear pore dilating agent trans-cyclohexane-1,2-diol in differentiated airway epithelium | The journal of gene medicine |
| 21982436 | 2012-02-15 | Contribution of flavonoids and catechol to the reduction of ICAM-1 expression in endothelial cells by a standardised Willow bark extract | Phytomedicine : international journal of phytotherapy and phytopharmacology |
| 22649749 | 2012-01-01 | Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis | Journal of analytical methods in chemistry |
| 21634386 | 2011-07-04 | Theoretical study of oxidation of cyclohexane diol to adipic anhydride by [Ru(IV)(O)(tpa)(H2O)]2+ complex (tpa ═ tris(2-pyridylmethyl)amine) | Inorganic chemistry |
| 21754205 | 2011-04-01 | (S)-2-Amino-2-(2-chloro-phen-yl)cyclo-hexa-none | Acta crystallographica. Section E, Structure reports online |
| 20717933 | 2011-03-01 | Exceptional structural and mechanical flexibility of the nuclear pore complex | Journal of cellular physiology |
| 21120472 | 2011-03-01 | Purification, characterization, and cloning of a bifunctional molybdoenzyme with hydratase and alcohol dehydrogenase activity | Applied microbiology and biotechnology |
| 21268602 | 2011-02-21 | Theoretical insights into heme-catalyzed oxidation of cyclohexane to adipic acid | Inorganic chemistry |
| 20429581 | 2010-06-04 | A very active cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides | The Journal of organic chemistry |
| 20413647 | 2010-06-01 | The mechanism of boron mobility in wheat and canola phloem | Plant physiology |
