cis-11-Eicosenamide

Base Information

• Chemical Name: cis-11-Eicosenamide
• CAS No.: 10436-08-5
• Molecular Formula: C20H39NO
• Molecular Weight: 309.536
• Hs Code.: 2924199090
• DSSTox Substance ID: DTXSID80338252
• Nikkaji Number: J740.353D
• ChEMBL ID: CHEMBL316405
• Mol file: 10436-08-5.mol

Synonyms:cis-11-Eicosenamide;10436-08-5;(Z)-icos-11-enamide;(Z)-11-Icosenamide;(11Z)-ICOS-11-ENAMIDE;gondamide;oleylacetamide;cis-11-icosenamide;(11Z)-icosenamide;(Z)-11-eicosenamide;(11Z)-11-eicosenamide;(11Z)-11-Icosenamide;(11Z)-11-Icosenamide #;CHEMBL316405;DTXSID80338252;CHEBI:146167;LBHQTVBKPMHICN-KTKRTIGZSA-N;AKOS037645100;AS-57100

Chemical Property of cis-11-Eicosenamide

Chemical Property:

• Vapor Pressure: 3.12E-08mmHg at 25°C
• Melting Point: 79 °C
• Refractive Index: 1.468
• Boiling Point: 448.4 °C at 760 mmHg
• PKA: 16.61±0.40(Predicted)
• Flash Point: 225 °C
• PSA: 43.09000
• Density: 0.876 g/cm³
• LogP: 6.98970
• XLogP3: 7.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 17
• Exact Mass: 309.303164868
• Heavy Atom Count: 22
• Complexity: 260

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCCCC(=O)N
• Isomeric SMILES: CCCCCCCC/C=C\CCCCCCCCCC(=O)N
• Uses: Cis-11-Eicosenamide is used in the biological study for its antigenotoxicity and cytotoxic potentials of metabiotics extracted from isolated probiotic Lactobacillus on human colon cancer cells.

Technology Process of cis-11-Eicosenamide

There total 3 articles about cis-11-Eicosenamide 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:

11-eicosenoic acid (5561-99-9) → cis-11-eicosenamide (10436-08-5)

Guidance literature:

With phosphorus trichloride; Behandeln des Reaktionsprodukts mit Ammoniak;

Reference yield:

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) → cis-11-eicosenamide (10436-08-5)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogen bromide / 140 °C

2: absolute ethanol / Verseifen der Reaktionsprodukte mit 50prozentiger KOH und Destillieren der erhaltenen Dicabonsaeure unter vermindertem Druck

3: PCl₃ / Behandeln des Reaktionsprodukts mit Ammoniak

With ethanol; hydrogen bromide; phosphorus trichloride;

Reference yield:

(Z)-1-bromo-9-octadecene (13044-38-7,62871-05-0,6110-53-8) → cis-11-eicosenamide (10436-08-5)

Guidance literature:

Multi-step reaction with 2 steps

1: absolute ethanol / Verseifen der Reaktionsprodukte mit 50prozentiger KOH und Destillieren der erhaltenen Dicabonsaeure unter vermindertem Druck

2: PCl₃ / Behandeln des Reaktionsprodukts mit Ammoniak

With ethanol; phosphorus trichloride;

upstream raw materials:

11-eicosenoic acid

oleoyl alcohol

(Z)-1-bromo-9-octadecene