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Home Other Building Blocks 10486-19-8
10486-19-8,MFCD00007018
Catalog No.:AA0035NQ

10486-19-8 | Tridecanal

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$62.00   $44.00
- +
5g
98%
in stock  
$106.00   $75.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0035NQ
Chemical Name:
Tridecanal
CAS Number:
10486-19-8
Molecular Formula:
C13H26O
Molecular Weight:
198.3449
MDL Number:
MFCD00007018
SMILES:
CCCCCCCCCCCCC=O
FEMA Number:
4335
Properties
Properties
 
BP:
132-136 °C8 mm Hg(lit.)  
Form:
Liquid  
MP:
15°C  
Refractive Index:
n20/D 1.437(lit.)  
Stability:
Air Sensitive  
Storage:
-20 ℃;  

Computed Properties
 
Complexity:
110  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
11  
XLogP3:
5.4  

Downstream Synthesis Route

[1]JournalofChemicalSciences,2012,vol.124,p.835-839

[2]JournaloftheChemicalSociety,1905,vol.87,p.1901

[3]Synlett,2004,p.2010-2012

[1]TetrahedronLetters,1986,vol.27,p.2287-2290

[2]TetrahedronLetters,1986,vol.27,p.2287-2290

[1]OrganicLetters,2015,vol.17,p.3194-3197

[2]JournalofOrganicChemistry,2006,vol.71,p.6686-6689

[3]Tetrahedron,2003,vol.59,p.6739-6750

[4]ChemistryLetters,2002,p.250-251

[5]BulletinoftheChemicalSocietyofJapan,2003,vol.76,p.1433-1440

[6]TetrahedronLetters,2003,vol.44,p.9201-9204

[7]BulletinoftheChemicalSocietyofJapan,1990,vol.63,p.1888-1893

[8]JournaloftheIndianChemicalSociety,1989,vol.66,p.632-638

[9]JournalofOrganicChemistry,1997,vol.62,p.5664-5665

[10]Synlett,2004,p.2010-2012

[11]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.451-456

[12]AdvancedSynthesisandCatalysis,2006,vol.348,p.877-880

[13]TetrahedronLetters,1986,vol.27,p.2287-2290

[14]Patent:US2006/270634,2006,A1.Locationinpatent:Page/Pagecolumn2;sheet2

[15]JournalofAntibiotics,2018,vol.71,p.234-239

[16]AngewandteChemie-InternationalEdition,2020,vol.59,p.2360-2364    Angew.Chem.,2020,vol.132,p.2380-2384,5

[1]JournalofOrganicChemistry,1993,vol.58,p.3828-3839

[1]JournalofOrganicChemistry,1993,vol.58,p.3828-3839

Literature

Title: Functional evolution of duplicated odorant-binding protein genes, Obp57d and Obp57e, in Drosophila.

Journal: PloS one 20120101

Title: Potentially important nighttime heterogeneous chemistry: NO3 with aldehydes and N2O5 with alcohols.

Journal: Physical chemistry chemical physics : PCCP 20110607

Title: Synthesis of N-substituted 2-[(1E)-alkenyl]-4-(1H)-quinolone derivatives as antimycobacterial agents against non-tubercular mycobacteria.

Journal: European journal of medicinal chemistry 20110601

Title: The location of olfactory receptors within olfactory epithelium is independent of odorant volatility and solubility.

Journal: BMC research notes 20110101

Title: Functionalization vs. fragmentation: n-aldehyde oxidation mechanisms and secondary organic aerosol formation.

Journal: Physical chemistry chemical physics : PCCP 20101114

Title: Chemical composition and antibacterial, antifungal and antioxidant activities of the flower oil of Retama raetam (Forssk.) Webb from Tunisia.

Journal: Natural product research 20100501

Title: Teratogenic effects of diatom metabolites on sea urchin Paracentrotus lividus embryos.

Journal: Marine drugs 20100101

Title: Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).

Journal: Journal of agricultural and food chemistry 20010501

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SDS
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