N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide

Base Information

• Chemical Name: N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide
• CAS No.: 113-48-4
• Deprecated CAS: 16916-65-7,16916-66-8,56195-42-7,70322-82-6
• Molecular Formula: C17H25NO2
• Molecular Weight: 275.391
• Hs Code.: 2925190090
• European Community (EC) Number: 204-029-1
• NSC Number: 406879,36678
• DSSTox Substance ID: DTXSID6032562
• Nikkaji Number: J5.134I
• Wikipedia: N-Octyl_bicycloheptene_dicarboximide
• Wikidata: Q6951386
• ChEMBL ID: CHEMBL1874490
• Mol file: 113-48-4.mol

Synonyms:ethylhexylbicycloheptene dicarboximide;MGK 264;MGK-264;N-(2-ethylhexyl)-5-norbornene-2,3-dicarboxamide;N-octylbicycloheptene dicarboximide

Chemical Property of N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide

Chemical Property:

• Appearance/Colour: yellow liquid
• Vapor Pressure: 8.35E-07mmHg at 25°C
• Melting Point: <-20oC
• Refractive Index: 1.527
• Boiling Point: 406.093 °C at 760 mmHg
• PKA: -7.53±0.20(Predicted)
• Flash Point: 168.353 °C
• PSA: 37.38000
• Density: 1.085 g/cm³
• LogP: 2.94780
• Storage Temp.: 0-6°C
• Water Solubility.: 15mg/L at 25℃
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 275.188529040
• Heavy Atom Count: 20
• Complexity: 412

Purity/Quality:

99% ^*data from raw suppliers

N-Octylbicycloheptenedicarboximide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 20/21/22-21
• Safety Statements: 26-36/37/39-36/37

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Other Insecticides
• Canonical SMILES: CCCCC(CC)CN1C(=O)C2C3CC(C2C1=O)C=C3

Technology Process of N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide

There total 1 articles about N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide 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:

2-Ethylhexylamine (104-75-6) + 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride (129-64-6) → (+/-)-2-(2-ethyl-hexyl)-(3ac,7ac)-3a,4,7,7a-tetrahydro-4r,7c-methano-isoindole-1,3-dione (113-48-4)

Guidance literature:

With toluene;

upstream raw materials:

2-Ethylhexylamine

3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride