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2-(HYDROXYMETHYL)CYCLOHEXANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5331-08-8

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5331-08-8 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 34, p. 3029, 1986 DOI: 10.1248/cpb.34.3029Synthesis, p. 811, 1976 DOI: 10.1055/s-1976-24214Tetrahedron Letters, 23, p. 4647, 1982 DOI: 10.1016/S0040-4039(00)85677-4

Check Digit Verification of cas no

The CAS Registry Mumber 5331-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5331-08:
(6*5)+(5*3)+(4*3)+(3*1)+(2*0)+(1*8)=68
68 % 10 = 8
So 5331-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c8-5-6-3-1-2-4-7(6)9/h6,8H,1-5H2

5331-08-8Relevant academic research and scientific papers

Synthesis of Potent and Selective HDAC6 Inhibitors Bearing a Cyclohexane- or Cycloheptane-Annulated 1,5-Benzothiazepine Scaffold

De Vreese, Rob,Galle, Lisa,Depetter, Yves,Franceus, Jorick,Desmet, Tom,Van Hecke, Kristof,Benoy, Veronick,Van Den Bosch, Ludo,D'hooghe, Matthias

, p. 128 - 136 (2017)

Selective inhibitors of histone deacetylase 6 (HDAC6) are an emerging class of pharmaceuticals due to the involvement of HDAC6 in different pathways related to neurodegenerative diseases, cancer, and immunology. Herein, the synthesis of ten new benzohydro

Preparation and characterization of magnetic graphene nanocomposite containing Cu(proline)2 as catalyst for asymmetric aldol reactions

Kooti,Kooshki,Nasiri

, p. 2641 - 2656 (2019/02/14)

A new catalyst has been prepared via immobilization of Cu(proline)2 complex onto the surface of magnetic graphene. The fabricated nanocatalyst was characterized by Fourier-transform infrared (FT-IR) spectroscopy, powder X-ray diffraction (PXRD) analysis, vibrating-sample magnetometry (VSM), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, transmission electron microscopy (TEM), inductively coupled plasma (ICP) techniques, and elemental analysis. Its catalytic performance was investigated in the aldol reaction using a mild and ecofriendly procedure. The synthesized nanocomposite, which contains Cu(II) center as Lewis acid, was found to be an efficient catalyst for asymmetric aldol reactions, affording corresponding aldol products in high yield and excellent enantiomeric excess (> 90?%). The examined catalyst was prepared from low-cost, easily available starting materials and can be readily isolated by magnetic decantation for recycling and reuse in consecutive reactions without significant loss of activity.

1,1,2,2-Tetrahydroperoxy-1,2-Diphenylethane: An efficient and high oxygen content oxidant in various oxidative reactions

Khosravi, Kaveh,Naserifar, Shirin

supporting information, p. 6584 - 6592 (2018/10/05)

Several oxidative approaches namely thiocyanation of aromatic compounds, epoxidation of alkenes, amidation of aromatic aldehydes, epoxidation of α β-unsaturated ketones, oxidation of sulfides to sulfoxides and sulfones, bayer-villeger reaction, bromination and iodation of aniline and phenol derivatives oxidative esterification, oxidation of pyridines and oxidation of secondary, allylic and benzyllic alcohols were carried out using 1,1,2,2-Tetrahydroperoxy-1,2-Diphenylethane as the potential solid oxidant which can be stored for several months without any loss in its activity. All of the procedures were accomplished via mild reaction conditions and the products were afforded in high yields and short reaction times.

Synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols or 3-amino alcohols using iodobenzene dichloride and sodium azide

He, Tian,Gao, Wen-Chao,Wang, Wei-Kun,Zhang, Chi

supporting information, p. 1113 - 1118 (2014/04/03)

A general and efficient method for the synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols and 3-amino alcohols has been developed using the same reagent combination of iodobenzene dichloride (PhICl2) and sodium azide (NaN3).

Chemoselective, iron(ii)-catalyzed oxidation of a variety of secondary alcohols over primary alcohols utilizing H2O2 as the oxidant

Lenze, Matthew,Bauer, Eike B.

, p. 5889 - 5891 (2013/07/19)

A mild, iron-based catalyst system is presented that selectively oxidizes secondary alcohols to the corresponding hydroxy ketones in the presence of primary alcohols within 15 minutes at room temperature, utilizing H 2O2 as the oxidant.

Catalyst-free selective oxidation of alcohols to carbonyls using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane as an efficient oxidant

Azarifar, Davood,Najminejad, Zohreh,Khosravi, Kaveh

, p. 979 - 983 (2013/09/23)

A simple and efficient method for the selective oxidation of alcohols to ketones using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane at room temperature is developed. The reactions were smoothly proceeded under catalyst-free conditions to provide ketones in quantitative yields within short reaction times. Also, this method is compatible with many functional groups including aldehydes, olefins, halogens, amines and esters. Graphical Abstract: [Figure not available: see fulltext.]

Lewis base catalysis by thiourea: N -bromosuccinimide-mediated oxidation of alcohols

Tripathi, Chandra Bhushan,Mukherjee, Santanu

experimental part, p. 1592 - 1598 (2012/03/11)

In recent times, (thio)urea derivatives have become synonymous with hydrogen bonding owing to their extensive applicability as small molecule organocatalysts. In this paper, another activation mode by thiourea derivatives, namely via Lewis base catalysis, is disclosed for the NBS-mediated oxidation of alcohols. The mild reaction conditions employed here is suitable for chemoselective oxidation of secondary alcohol in the presence of primary alcohol.

Direct asymmetric aldol reactions inspired by two types of natural aldolases: Water-compatible organocatalysts and ZnII complexes

Paradowska, Joanna,Pasternak, Monika,Gut, Bartosz,Gryzlo, Beata,Mlynarski, Jacek

scheme or table, p. 173 - 187 (2012/02/04)

In this article the utility of water-compatible amino-acid-based catalysts was explored in the development of diastereo- and enantioselective direct aldol reactions of a broad range of substrates. Chiral C2-symmetrical proline- and valine-based

Direct asymmetric α-hydroxymethylation of ketones in homogeneous aqueous solvents

Pasternak, Monika,Paradowska, Joanna,Rogozińska, Maria,Mlynarski, Jacek

scheme or table, p. 4088 - 4090 (2010/08/19)

A chiral prolinamide-based zinc complex promotes the aldol reaction of ketones with aqueous formaldehyde, giving the corresponding adducts in good yields and high ees. The efficient direct aldol reaction of formaldehyde with ketones in homogeneous aqueous

PHENYL SUBSTITUTED CYCLOALKYLAMINES AS MONOAMINE REUPTAKE INHIBITORS

-

Page/Page column 54, (2009/01/24)

Phenyl-substituted cyclohexylamine derivatives and method for their synthesis and characterization are disclosed. Use of these compounds to treat/prevent neurological disorders as well as methods for their synthesis are set forth herein. Exemplary compoun

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