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Home Other Building Blocks 112-12-9
112-12-9,MFCD00009583
Catalog No.:AA003RYQ

112-12-9 | Methyl Nonyl Ketone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
98%
in stock  
$17.00   $12.00
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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:
AA003RYQ
Chemical Name:
Methyl Nonyl Ketone
CAS Number:
112-12-9
Molecular Formula:
C11H22O
Molecular Weight:
170.2918
MDL Number:
MFCD00009583
SMILES:
CCCCCCCCCC(=O)C
Properties
Properties
 
BP:
230.8°C at 760 mmHg  
Form:
Liquid  
MP:
11-13 °C(lit.)  
Refractive Index:
n20/D 1.43(lit.)  
Storage:
Keep in dry area;Room Temperature;  


Downstream Synthesis Route

[1]JournalofOrganicChemistry,1990,vol.55,p.462-466

[2]JournalofOrganicChemistry,1998,vol.63,p.7576-7577

[3]TetrahedronLetters,2012,vol.53,p.5880-5882,3

[4]ChemistryLetters,2001,p.922-923

[5]BulletinoftheChemicalSocietyofJapan,2004,vol.77,p.1905-1914

[6]JournaloftheChineseChemicalSociety,2008,vol.55,p.229-232

[7]JournalofOrganicChemistry,1991,vol.56,p.2416-2421

[8]ChemicalCommunications,2000,p.1245-1246

[9]BulletinoftheChemicalSocietyofJapan,1999,vol.72,p.2287-2306

[10]JournalofOrganometallicChemistry,2001,vol.624,p.344-347

[11]RussianJournalofOrganicChemistry,2005,vol.41,p.1752-1754

[12]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2006,vol.45,p.564-567

[13]JournalofOrganicChemistry,1999,vol.64,p.2433-2439

[14]JournalofOrganicChemistry,2011,vol.76,p.8955-8961

[15]AngewandteChemie-InternationalEditioninEnglish,1997,vol.36,p.2208-2210

[16]Tetrahedron,2008,vol.64,p.10761-10766

[17]BulletinoftheChemicalSocietyofJapan,1986,vol.59,p.3297-3298

[18]EuropeanJournalofOrganicChemistry,2001,p.1235-1247

[19]ChemPlusChem,2013,vol.78,p.101-116

[20]DaltonTransactions,2011,vol.40,p.7617-7631

[21]JournaloftheAmericanChemicalSociety,1949,vol.71,p.2828    Chem.Abstr.,1948,p.7313

[22]OrganicLetters,2004,vol.6,p.441-443

[23]JournalofOrganicChemistry,2004,vol.69,p.6851-6859

[24]AdvancedSynthesisandCatalysis,2005,vol.347,p.677-688

[25]AdvancedSynthesisandCatalysis,2005,vol.347,p.677-688

[26]Tetrahedron,2005,vol.61,p.12058-12064

[27]PolishJournalofChemistry,2005,vol.79,p.1963-1965

[28]TetrahedronLetters,2004,vol.45,p.4249-4251

[29]Patent:US5912388,1999,A

[30]AppliedOrganometallicChemistry,2014,vol.28,p.576-583

[31]ChemCatChem,2016,vol.8,p.2704-2709

[32]JournalofOrganicChemistry,2017,vol.82,p.6671-6679

[33]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.1359-1363

[34]ChemicalCommunications,2018,vol.54,p.10164-10167

[35]Synlett,2019,vol.30,p.315-318

[1]Houben[ChemischeBerichte,1902,vol.35,p.3591]

[1]AngewandteChemie-InternationalEdition,1998,vol.37,p.2347-2349

[2]Synthesis,2002,p.279-291

[3]AngewandteChemie-InternationalEdition,2019,vol.58,p.6727-6731    Angew.Chem.,2019,vol.131,p.6799-6803,5

[4]ChemCatChem,2017,vol.9,p.80-83

[5]Catalysisscienceandtechnology,2013,vol.3,p.81-84

[6]AdvancedSynthesisandCatalysis,2014,vol.356,p.1093-1097

[7]OrganicLetters,2017,vol.19,p.3656-3659

[8]Tetrahedron,2000,vol.56,p.2153-2166

[9]JournalofOrganicChemistry,1984,vol.49,p.2438-2443

[10]CatalysisCommunications,2017,vol.92,p.1-4

[11]AdvancedSynthesisandCatalysis,2012,vol.354,p.2619-2624

[12]JournalofOrganicChemistry,1981,vol.46,p.5344-5348

[13]AdvancedSynthesisandCatalysis,2018,vol.360,p.676-681

[14]InorganicaChimicaActa,2012,vol.380,p.301-307

[15]Organometallics,2018,vol.37,p.1271-1279

[16]OrganicLetters,2001,vol.3,p.3421-3424

[17]ChemistryLetters,1987,p.1331-1334

[18]ChemischeBerichte,1936,vol.69,p.1782

[19]IndustrialandEngineeringChemistry,1944,vol.36,p.611

[20]BulletindelaSocieteChimiquedeFrance,1937,vol.<5>4,p.31,41

[21]BulletindelaSocieteChimiquedeFrance,1937,vol.<5>4,p.31,41

[22]BulletindelaSocieteChimiquedeFrance,1937,vol.<5>4,p.31,41

[23]BulletindelaSocieteChimiquedeFrance,1937,vol.<5>4,p.31,41

[24]ChemischeBerichte,1902,vol.35,p.3591

[25]BulletindelaSocieteChimiquedeFrance,1925,vol.<4>37,p.872,873

[26]JournaloftheAmericanChemicalSociety,1953,vol.75,p.897,899

[27]ChemischeBerichte,1902,vol.35,p.3591

[28]JournaloftheChemicalSociety,1911,vol.99,p.55,71    JournaloftheChemicalSociety,1914,vol.105,p.1121,1123,1128

[29]JustusLiebigsAnnalenderChemie,1973,p.1179-1194

[30]JournaloftheAmericanChemicalSociety,1974,vol.96,p.5290-5291

[31]CanadianJournalofChemistry,1990,vol.68,p.720-724

[32]ChemistryLetters,1983,p.1647-1648

[33]JournaloftheChemicalSociety.Chemicalcommunications,1985,p.501-502

[34]BulletinoftheChemicalSocietyofJapan,2004,vol.77,p.1905-1914

[35]TetrahedronAsymmetry,2010,vol.21,p.566-570

[1]GazzettaChimicaItaliana,1968,vol.98,p.139-146

[1]Citterio,Attilio;Ferrario,Francesco;Bernardinis,SilviaDe[JournalofChemicalResearch,Miniprint,1983,#12,p.2669-2683]

Literature

Title: Melkina OE, et al. Ketones 2-heptanone, 2-nonanone, and 2-undecanone inhibit DnaK-dependent refolding of heat-inactivated bacterial luciferases in Escherichia coli cells lacking small chaperon IbpB. Appl Microbiol Biotechnol. 2017 Jul;101(14):5765-5771.

Title: Lou Y, et al. Houttuynia cordata Thunb. and its bioactive compound 2-undecanone significantly suppress benzo(a)pyrene-induced lung tumorigenesis by activating the Nrf2-HO-1/NQO-1 signaling pathway. J Exp Clin Cancer Res. 2019 Jun 7;38(1):242.

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