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
Canonical 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
118-120ºC (10 mmHg)
Melting Point
73-77ºC
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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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