Cyclononene

Base Information

• Chemical Name: Cyclononene
• CAS No.: 933-21-1
• Molecular Formula: C9H16
• Molecular Weight: 124.226
• Hs Code.: 2914299000
• European Community (EC) Number: 806-412-4
• DSSTox Substance ID: DTXSID201316842
• Nikkaji Number: J80.023F,J79.823A
• Wikipedia: Cyclononene
• Wikidata: Q15147831
• Mol file: 933-21-1.mol

Synonyms:Cyclononene;(Z)-Cyclononene;1-Cyclononene;933-21-1;1-Cyclononene #;cis-Cyclononene;(1Z)-Cyclononene;Cyclononene, (Z)-;BESIOWGPXPAVOS-UHFFFAOYSA-N;BESIOWGPXPAVOS-UPHRSURJSA-N;DTXSID201316842;3618-11-9;AKOS024436732;Q15147831

Chemical Property of Cyclononene

Chemical Property:

• Vapor Pressure: 2.08mmHg at 25°C
• Refractive Index: 1.4805
• Boiling Point: 169°Cat760mmHg
• Flash Point: 41.2°C
• PSA: 0.00000
• Density: 0.812g/cm³
• LogP: 3.28690
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 124.125200510
• Heavy Atom Count: 9
• Complexity: 72

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCCC=CCCC1
• Isomeric SMILES: C1CCC/C=C\CCC1

Technology Process of Cyclononene

There total 7 articles about Cyclononene 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:

(E)-cyclononene (3958-38-1) → nona-1,8-diene (4900-30-5) + (Z)-cyclononene (933-21-1)

Guidance literature:

at 500 ℃;

DOI:10.1021/ja01570a055

Reference yield:

dithiocarbonic acid O-cyclononyl ester-S-methyl ester (99992-31-1) → nona-1,8-diene (4900-30-5) + (Z)-cyclononene (933-21-1)

Guidance literature:

at 500 ℃; Pyrolysis;

DOI:10.1021/ja01570a055

Reference yield:

cis-bicyclo[6.1.0]nonane (13757-43-2) → nona-1,8-diene (4900-30-5) + (E)-cyclononene (3958-38-1) + (Z)-cyclononene (933-21-1)

Guidance literature:

In pentane; Product distribution; Mechanism; Irradiation;

DOI:10.1021/jo00322a052

upstream raw materials:

(E)-cyclononene

dithiocarbonic acid O-cyclononyl ester-S-methyl ester

cyclononane

cis-bicyclo[6.1.0]nonane

Downstream raw materials:

cyclononanone

cyclononylidene-2,4,6-trinitroaniline

nona-1,8-diene

Refernces

• 1、 Kirmse, Wolfgang,Hellwig, Georg. "Deamination Reactions, 37. Decomposition of Bicyclononane- and Bicyclonon-2-ene-9-diazonium Ions". . p. 2744 - 2754. Retrieved 2007/10/02.