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334-49-6,MFCD00039530
Catalog No.:AA0035MW

334-49-6 | Trans-2-decenoic acid

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1g
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$37.00   $26.00
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5g
95%
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$89.00   $62.00
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10g
95%
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$155.00   $109.00
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25g
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$311.00   $218.00
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100g
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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:
AA0035MW
Chemical Name:
Trans-2-decenoic acid
CAS Number:
334-49-6
Molecular Formula:
C10H18O2
Molecular Weight:
170.2487
MDL Number:
MFCD00039530
SMILES:
CCCCCCC/C=C/C(=O)O
FEMA Number:
3913
Properties
Properties
 
BP:
278.6±9.0°C at 760 mmHg  
Form:
Liquid  
MP:
18.83°C (estimate)  
Refractive Index:
1.46-1.464  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
139  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
7  
XLogP3:
3.8  

Downstream Synthesis Route

[1]Tanaka,Shinji;Kon,Yoshihiro;Uesaka,Yumiko;Morioka,Ryo;Tamura,Masanori;Sato,Kazuhiko[ChemistryLetters,2016,vol.45,#2,p.188-190]

[2]Gouge[AnnalesdeChimie(Cachan,France),1951,vol.<12>6,p.648,682]

[3]Lehtinen,Christel;Nevalainen,Vesa;Brunow,Gösta[Tetrahedron,2000,vol.56,#47,p.9375-9382]

[4]Kandagatla,SuneelK.;Mack,Todd;Simpson,Sean;Sollenberger,Jill;Helton,Eric;Raner,GregoryM.[Chemico-BiologicalInteractions,2014,vol.219,p.195-202]

[5]Brodl,Eveline;Ivkovic,Jakov;Tabib,ChaitanyaR.;Breinbauer,Rolf;Macheroux,Peter[BioorganicandMedicinalChemistry,2017,vol.25,#4,p.1487-1495]

[6]CurrentPatentAssignee:NATIONALINSTITUTEOFADVANCEDINDUSTRIALSCIENCEANDTECHNOLOGY-JP2016/204318,2016,ALocationinpatent:Paragraph0040-0050

[1]Böttcher,Thomas;Dieterich,CoraLisbeth;Prothiwa,Michaela;Szamosvári,Dávid[ChemicalCommunications,2020,vol.56,#47,p.6328-6331]

[2]Szamosvári,Dávid;Böttcher,Thomas[AngewandteChemie-InternationalEdition,2017,vol.56,#25,p.7271-7275][Angew.Chem.,2017,vol.129,#25,p.7377-7381,5]

[3]CurrentPatentAssignee:UNIVERSITÄTKONSTANZ-EP3260445,2017,A1Locationinpatent:Paragraph0114;0115;0116

[4]Boehme,Roswitha;Jung,Guenther;Breitmaier,Eberhard[HelveticaChimicaActa,2005,vol.88,#11,p.2837-2841]

[5]Marquardt;Schmid;Jung[Synlett,2000,#8,p.1131-1132]

[6]Galleano,Iacopo;Schiedel,Matthias;Jung,Manfred;Madsen,AndreasS.;Olsen,ChristianA.[JournalofMedicinalChemistry,2016,vol.59,#3,p.1021-1031]

[7]Galleano,Iacopo;Schiedel,Matthias;Jung,Manfred;Madsen,AndreasS.;Olsen,ChristianA.[JournalofMedicinalChemistry,2016,vol.59,#6,p.2847-2847]

[8]Tulus[IstanbulUniversitesiFenFakultesiMecmuasi,SeriA:Matematik-Fizik-Kimya,1944,vol.9,p.105][Chem.Abstr.,1946,p.3722]Thaler;Eisenlohr[BiochemischeZeitschrift,1941,vol.308,p.96,97]Zaar[BerichtvonSchimmelandCo.,1929,p.307]

[9]Matveeva;Erin;Kurz[RussianJournalofOrganicChemistry,1997,vol.33,#8,p.1065-1067]

[10]Bonnard,Isabelle;Rolland,Marc;Salmon,Jean-Marie;Debiton,Eric;Barthomeuf,Chantal;Banaigs,Bernard[JournalofMedicinalChemistry,2007,vol.50,#6,p.1266-1279]

[11]Kemme,SusanneT.;Smejkal,Tomas;Breit,Bernhard[Chemistry-AEuropeanJournal,2010,vol.16,#11,p.3423-3433]

[1]Bonnard,Isabelle;Rolland,Marc;Salmon,Jean-Marie;Debiton,Eric;Barthomeuf,Chantal;Banaigs,Bernard[JournalofMedicinalChemistry,2007,vol.50,#6,p.1266-1279]

[1]Song,Jiangao;Hesse,Manfred[Tetrahedron,1993,vol.49,#31,p.6797-6804]

[2]CurrentPatentAssignee:NIPPONZOKIPHARMACEUTICALCO.,LTD;NAGOYAINDUSTRIALSCIENCERESEARCHINSTITUTE-EP2457567,2015,B1

334-49-6   
C6H14-EtOAc 
 
chlorideoftrans-2-decenicacid 
  7367-88-6 

[1]CurrentPatentAssignee:NIPPONZOKIPHARMACEUTICALCO.,LTD;NAGOYAINDUSTRIALSCIENCERESEARCHINSTITUTE-EP2204172,2010,A1

Literature

Title: Naumowicz M, Petelska AD, Figaszewski ZA.Impedance analysis of complex formation equilibria in phosphatidylcholine bilayers containing decanoic acid or decylamine.Cell Biochem Biophys. 2011 Sep;61(1):145-55.

Title: Kumar A, Singh S, Jain S, Kumar P.Synthesis, antimicrobial evaluation, QSAR and in Silico ADMET studies of decanoic acid derivatives.Acta Pol Pharm. 2011 Mar-Apr;68(2):191-204.

Title: Petelska AD, Figaszewski ZA.Interfacial tension of the lipid membrane formed from phosphatidylcholine-decanoic acid and phosphatidylcholine-decylamine systems.J Membr Biol. 2011 May;241(2):103-8.

Title: Hattori N et al.Royal jelly and its unique fatty acid, 10-hydroxy-trans-2-decenoic acid, promote neurogenesis by neural stem/progenitor cells in vitro. Biomed Res. 2007 Oct;28(5):261-6.

Title: Suzuki KM et al. Estrogenic activities of Fatty acids and a sterol isolated from royal jelly. Evid Based Complement Alternat Med. 2008 Sep;5(3):295-302.

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