Catalog No.:AA00368J

874-23-7 | 2-Acetylcyclohexanone

Name: Name:2-Acetylcyclohexanone
Brand: AABLOCKS
SKU: AA00368J
Availability: InStock
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98%

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$11.00 $8.00

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98%

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$17.00 $12.00

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10g

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25g

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00368J

Chemical Name:

2-Acetylcyclohexanone

CAS Number:

874-23-7

Molecular Formula:

C8H12O2

Molecular Weight:

140.1797

MDL Number:

MFCD00001633

SMILES:

O=C1CCCCC1C(=O)C

NSC Number:

7713

Properties

BP:

257.1°C at 760 mmHg

Form:

Liquid

MP:

-11°C

Refractive Index:

n20/D 1.509(lit.)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

161

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Undefined Atom Stereocenter Count:

XLogP3:

0.9

Downstream Synthesis Route

874-23-7

141-52-6

506-93-4

58544-43-7

[1]Mitter;Bhattacharya[JournaloftheIndianChemicalSociety,1927,vol.4,p.156][ChemischesZentralblatt,1927,vol.98,#II,p.1703]

[2]Mitter;Bhattacharya[QuarterlyJournaloftheIndianChemicalSociety,vol.4,p.152,153][ChemischesZentralblatt,1927,vol.98,#II,p.1703]

874-23-7

506-93-4

58544-43-7

[1]Mitter;Bhattacharya[JournaloftheIndianChemicalSociety,1927,vol.4,p.156][ChemischesZentralblatt,1927,vol.98,#II,p.1703]

874-23-7

14112-98-2

[1]EuropeanJournalofOrganicChemistry,2010,p.2861-2866

[2]ChemicalPapers,2021,vol.75,p.3575-3586

[3]JournaloftheChemicalSociety.PerkintransactionsI,1990,p.1423-1427

[4]JournalofMedicinalChemistry,1983,vol.26,p.492-499

[5]AdvancedSynthesisandCatalysis,2015,vol.357,p.4063-4068

[6]JournaloftheAmericanChemicalSociety,1948,vol.70,p.4023,4025

[7]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1905,vol.141,p.1033 AnnalesdeChimie(Cachan,France),1912,vol.<8>26,p.234

[8]JournaloftheAmericanChemicalSociety,1963,vol.85,p.3752-3753

[9]JournaloftheAmericanChemicalSociety,1988,vol.110,p.5203-5205

[10]TetrahedronAsymmetry,1992,vol.3,p.1523-1524

874-23-7

64229-97-6

[1]Tetrahedron,2008,vol.64,p.5191-5199

[2]Synthesis,2005,p.1136-1140

[3]Synthesis,2011,p.347-351

[4]ChemicalCommunications,2009,p.6991-6993

[5]OrganicLetters,2014,vol.16,p.600-603

[6]TetrahedronLetters,2009,vol.50,p.473-475

[7]OrganicandBiomolecularChemistry,2012,vol.10,p.4327-4329

[8]JournaloftheChemicalSociety,1957,p.4419,4423

[9]BulletinoftheChemicalSocietyofJapan,1977,vol.50,p.1831-1835

[10]CatalysisLetters,2016,vol.146,p.570-574

108-94-1

108-24-7

874-23-7

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,2005,vol.180,p.109-116

[2]Patent:EP2157088,2010,A1.Locationinpatent:Page/Pagecolumn38-39

[3]JournaloftheAmericanChemicalSociety,1945,vol.67,p.284

Literature

Title: Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects. Current knowledge assembled at an international workshop at BfR, Germany.

Journal: Cellular and molecular life sciences : CMLS 20120301

Title: 8-Azatetracyclines: synthesis and evaluation of a novel class of tetracycline antibacterial agents.

Journal: Journal of medicinal chemistry 20110310

Title: Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

Journal: Organic & biomolecular chemistry 20100307

Title: Tautomerization of 2-acetylcyclohexanone. 1. Characterization of keto-enol/enolate equilibria and reaction rates in water.

Journal: The Journal of organic chemistry 20030404

Title: Nitrosation of 2-acetylcyclohexanone. 2. Reaction in water in the absence and presence of cyclodextrins.

Journal: The Journal of organic chemistry 20030404

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