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1125-21-9,MFCD00043119
Catalog No.:AA007T0Y

1125-21-9 | 2,6,6-Trimethyl-2-cyclohexene-1,4-dione

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5g
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25g
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$39.00   $27.00
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$84.00   $59.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA007T0Y
Chemical Name:
2,6,6-Trimethyl-2-cyclohexene-1,4-dione
CAS Number:
1125-21-9
Molecular Formula:
C9H12O2
Molecular Weight:
152.1904
MDL Number:
MFCD00043119
SMILES:
O=C1C=C(C)C(=O)C(C1)(C)C
FEMA Number:
3421
Properties
Computed Properties
 
Complexity:
246  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
1  

Downstream Synthesis Route

[1]Patent:CN109456153,2019,A.Locationinpatent:Paragraph0048-0062;0064

[2]HelveticaChimicaActa,1956,vol.39,p.2041,2046    JustusLiebigsAnnalenderChemie,1957,vol.603,p.129,137

[3]Tetrahedron,Supplement,1966,vol.8,p.1-7

[4]AgriculturalandBiologicalChemistry,1981,vol.45,p.791-794

[5]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.80-84

[1]Synthesis,2013,vol.45,p.615-620

[2]ChemicalCommunications,2015,vol.51,p.5852-5855

[3]Patent:CN105601490,2016,A.Locationinpatent:Paragraph0017;0018

[4]OrganicLetters,2006,vol.8,p.3149-3151

[5]ChemistryLetters,1984,p.2031-2032

[6]ChemischeBerichte,1987,vol.120,p.1133-1150

[7]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.6472-6478

[8]TetrahedronLetters,1988,vol.29,p.765-768

[9]ChemistryLetters,1983,p.1081-1082

[10]ChemistryLetters,1983,p.1081-1082

[11]Chemistry-AEuropeanJournal,2005,vol.11,p.3899-3914

[12]AdvancedSynthesisandCatalysis,2011,vol.353,p.1447-1451

[13]BulletinoftheKoreanChemicalSociety,2012,vol.33,p.459-463

[14]RSCAdvances,2016,vol.6,p.90887-90896

[15]Patent:CN105481671,2016,A.Locationinpatent:Paragraph0008;0009

[16]ChemCatChem,2017,vol.9,p.3821-3826

[17]Patent:CN108911954,2018,A.Locationinpatent:Paragraph0037;0038;0045;0046;0053;0054;0061;0062

[18]Catalysisscienceandtechnology,2019,vol.9,p.1398-1405

[1]TetrahedronAsymmetry,1992,vol.3,p.443-450

[2]OrganicandBiomolecularChemistry,2006,vol.4,p.4186-4192

896107-70-3    78-59-1    20547-99-3    1125-21-9    13215-88-8   
megastigmatrienone 

[1]Strauss,ChristopherR.;Wilson,Bevan;Williams,PatrickJ.[Phytochemistry,1987,vol.26,#7,p.1995-1998]

[1]HelveticaChimicaActa,1989,vol.72,p.365-369

[2]Patent:WO2010/147653,2010,A1.Locationinpatent:Page/Pagecolumn157

Literature

Title: Enoate reductases from non conventional yeasts: bioconversion, cloning, and functional expression in Saccharomyces cerevisiae.

Journal: Journal of biotechnology 20111220

Title: Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.

Journal: Bioresource technology 20110301

Title: Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans.

Journal: Applied microbiology and biotechnology 20110101

Title: Volatile compounds in honey: a review on their involvement in aroma, botanical origin determination and potential biomedical activities.

Journal: International journal of molecular sciences 20110101

Title: Composition of sulla (Hedysarum coronarium L.) honey solvent extractives determined by GC/MS: norisoprenoids and other volatile organic compounds.

Journal: Molecules (Basel, Switzerland) 20100909

Title: Volatile composition screening of Salix spp. nectar honey: benzenecarboxylic acids, norisoprenoids, terpenes, and others.

Journal: Chemistry & biodiversity 20100901

Title: Quality and functionality of saffron: quality control, species assortment and affinity of extract and isolated saffron compounds to NMDA and sigma1 (sigma-1) receptors.

Journal: Planta medica 20080601

Title: Ketoisophorone transformation by Marchantia polymorpha and Nicotiana tabacum cultured cells.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20080101

Title: A variety of volatile compounds as markers in unifloral honey from dalmatian sage (Salvia officinalis L.).

Journal: Chemistry & biodiversity 20061201

Title: Generation of aroma compounds from Ditaxis heterantha by Saccharomyces cerevisiae.

Journal: Applied microbiology and biotechnology 20060801

Title: In situ product recovery (ISPR) by crystallization: basic principles, design, and potential applications in whole-cell biocatalysis.

Journal: Applied microbiology and biotechnology 20060601

Title: Use of SPME-GC-MS in the study of time evolution of the constituents of saffron aroma: modifications of the composition during storage.

Journal: Journal of chromatographic science 20060101

Title: Cloning and overexpression of the old yellow enzyme gene of Candida macedoniensis, and its application to the production of a chiral compound.

Journal: Journal of biotechnology 20041019

Title: Anthropogenic organic contaminants in sediments of the Lippe river, Germany.

Journal: Water research 20040901

Title: In situ product removal using a crystallization loop in asymmetric reduction of 4-oxoisophorone by Saccharomyces cerevisiae.

Journal: Biotechnology and bioengineering 20040630

Title: Molecular markers of anthropogenic activity in sediments of the Havel and Spree Rivers (Germany).

Journal: Water research 20030601

Title: Old Yellow Enzyme from Candida macedoniensis catalyzes the stereospecific reduction of the C=C bond of ketoisophorone.

Journal: Bioscience, biotechnology, and biochemistry 20021201

Title: Chemicals with sweet aroma descriptors found in Portuguese wines from the Douro region: 2,6,6-trimethylcyclohex-2-ene-1,4-dione and diacetyl.

Journal: Journal of agricultural and food chemistry 20010101

Title: Hegazy ME, et al. Ketoisophorone transformation by Marchantia polymorpha and Nicotiana tabacum cultured cells. Z Naturforsch C. 2008 May-Jun;63(5-6):403-8.

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Tags:1125-21-9 Molecular Formula|1125-21-9 MDL|1125-21-9 SMILES|1125-21-9 2,6,6-Trimethyl-2-cyclohexene-1,4-dione