2,6,10-Trimethylundec-9-enal

Base Information

• Chemical Name: 2,6,10-Trimethylundec-9-enal
• CAS No.: 141-13-9
• Molecular Formula: C14H26 O
• Molecular Weight: 210.36
• European Community (EC) Number: 205-460-8
• NSC Number: 122698
• UNII: JNM5JFE28J
• DSSTox Substance ID: DTXSID7051711
• Nikkaji Number: J12.264E
• Wikidata: Q2166066
• Mol file: 141-13-9.mol

Synonyms:2,6,10-Trimethylundec-9-enal;Adoxal;141-13-9;Farenal;Doxal;9-Undecenal, 2,6,10-trimethyl-;2,6,10-Trimethyl-9-undecenal;Trimethyl undecylenic aldehyde;2,6,10-Trimethyl-9-undecen-1-al;EINECS 205-460-8;UNII-JNM5JFE28J;JNM5JFE28J;NSC 122698;AI3-36109;NSC-122698;9-Undecenal,2,6,10-trimethyl-;SCHEMBL229925;9-Undecenal,6,10-trimethyl-;DTXSID7051711;FEMA NO. 4768;2,10-Trimethyl-9-undecen-1-al;9-undecenal, 2,6,10-trimetil-;2,6,10-Trimethyl-9-undecenal #;NSC122698;2,6,10 - trimethylundec - 9 - enal;J12.264E;LS-158502;FT-0626380;Q2166066

Chemical Property of 2,6,10-Trimethylundec-9-enal

Chemical Property:

• Appearance/Colour: Colourless to pale yellow liquid
• Vapor Pressure: 0.00257mmHg at 25°C
• Melting Point: 15°C (estimate)
• Refractive Index: 1.4557 (estimate)
• Boiling Point: 286.9 °C at 760 mmHg
• Flash Point: 130.5 °C
• PSA: 17.07000
• Density: 0.837 g/cm³
• LogP: 4.37420
• Water Solubility.: 670μg/L at 20℃
• XLogP3: 5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 210.198365449
• Heavy Atom Count: 15
• Complexity: 190

Purity/Quality:

99.9% ^*data from raw suppliers

2,6,10-TRIMETHYL-9-UNDECENAL 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CCCC(C)C=O)CCC=C(C)C
• Uses: Perfume.

Technology Process of 2,6,10-Trimethylundec-9-enal

There total 1 articles about 2,6,10-Trimethylundec-9-enal which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 51.1%

glycidic acid (65416-34-4) → 2,6,10-trimethylundec-9-enal (141-13-9)

Guidance literature:

In n-heptane; at 280 ℃;

upstream raw materials:

glycidic acid

Refernces