CAS 1792-81-0 | 1,2-Cyclohexanediol, (1R,2S)-rel- | CAS Number 1792-81-0

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1792-81-0 | 1,2-Cyclohexanediol, (1R,2S)-rel-

CAS No: 1792-81-0 Catalog No: AG0026V5 MDL No:MFCD00064944

Product Description

Catalog Number:

AG0026V5

Chemical Name:

1,2-Cyclohexanediol, (1R,2S)-rel-

CAS Number:

1792-81-0

Molecular Formula:

C6H12O2

Molecular Weight:

116.1583

MDL Number:

MFCD00064944

IUPAC Name:

(1R,2S)-cyclohexane-1,2-diol

InChI:

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

InChI Key:

PFURGBBHAOXLIO-OLQVQODUSA-N

SMILES:

O[C@@H]1CCCC[C@@H]1O

Properties

Complexity:

62.9

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

116.084g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

116.16g/mol

Monoisotopic Mass:

116.084g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

40.5A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

0.2

Literature

Title	Journal
Assessment of the nuclear pore dilating agent trans-cyclohexane-1,2-diol in differentiated airway epithelium.	The journal of gene medicine 20120701
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 20110704
A very active cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides.	The Journal of organic chemistry 20100604
On the origins of kinetic resolution of cyclohexane-1,2-diols through stereoselective acylation by chiral tetrapeptides.	Organic letters 20090806
From simple diols to carbohydrate derivatives of phenylarsonic acid.	Inorganic chemistry 20090202
Oxidation of cyclohexanediol derivatives with 12-tungstophosphoric acid-hydrogen peroxide system.	Journal of oleo science 20090101
Advantages of synthesizing trans-1,2-cyclohexanediol in a continuous flow microreactor over a standard glass apparatus.	The Journal of organic chemistry 20071221
Biocatalytic production of enantiopure cyclohexane-trans-1,2-diol using extracellular lipases from Bacillus subtilis.	Applied microbiology and biotechnology 20061001
Absence of interactive effects of trans-1,2-cyclohexanediol, a major metabolite of the side-chain of candesartan cilexetil, on digoxin-induced arrhythmias in dogs.	Journal of pharmacological sciences 20030801
Tin(II) chloride catalyzed reactions of diazodiphenylmethane with vicinal diols in an aprotic solvent. The reactions with cis- and trans-1,2-cyclohexanediols and 1,2-propanediol.	Carbohydrate research 20030422
Expression of benzene dioxygenase from Pseudomonas putida ML2 in cis-1,2-cyclohexanediol-degrading pseudomonads.	Applied microbiology and biotechnology 20010601
Asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids using (S,S)-cyclohexane-1,2-diol as a chiral auxiliary.	The Journal of organic chemistry 20010420