4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)-

Base Information

• Chemical Name: 4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)-
• CAS No.: 73839-58-4
• Molecular Formula: C₁₆H₂₅N₃O₂
• Molecular Weight: 291.393
• DSSTox Substance ID: DTXSID90224359
• Wikidata: Q76155499
• Mol file: 73839-58-4.mol

Synonyms:4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)-;N-(N'-4-Methylpiperazinopropyl)-cis-delta(sup 4)-tetrahydrophthalimide;cis-N-(3-(4-Methyl-1-piperazinyl)propyl)-4-cyclohexene-1,2-dicarboximide;73839-58-4;DTXSID90224359;LS-57471;1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-[3-(4-methyl-1-piperazinyl)propyl]-, cis-

Chemical Property of 4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)-

Chemical Property:

• Vapor Pressure: 1.4E-08mmHg at 25°C
• Boiling Point: 458.2°C at 760 mmHg
• Flash Point: 201.4°C
• Density: 1.135g/cm³
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 291.19467705
• Heavy Atom Count: 21
• Complexity: 415

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CN1CCN(CC1)CCCN2C(=O)C3CC=CCC3C2=O
• Isomeric SMILES: CN1CCN(CC1)CCCN2C(=O)[C@@H]3CC=CC[C@@H]3C2=O

Technology Process of 4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)-

There total 3 articles about 4-Cyclohexene-1,2-dicarboximide, N-(3-(4-methyl-1-piperazinyl)propyl)-, (Z)- 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:

1-methyl-piperazine (109-01-3) → 2-[3-(4-methyl-piperazino)-propyl]-(3ar,7ac)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione (73839-58-4)

Guidance literature:

Multi-step reaction with 3 steps

1: benzene

2: LiAlH₄; diethyl ether

3: 190 °C

With lithium aluminium tetrahydride; diethyl ether; benzene;

DOI:10.1021/jo01364a014

Reference yield:

3-(4-methylpiperazin-1-yl)propanenitrile (4491-92-3) → 2-[3-(4-methyl-piperazino)-propyl]-(3ar,7ac)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione (73839-58-4)

Guidance literature:

Multi-step reaction with 2 steps

1: LiAlH₄; diethyl ether

2: 190 °C

With lithium aluminium tetrahydride; diethyl ether;

DOI:10.1021/jo01364a014

Reference yield:

3-(N-methylpiperazino)propylamine (4572-03-6) + cis-1,2,3,6-tetrahydrophthalic anhydride (935-79-5) → 2-[3-(4-methyl-piperazino)-propyl]-(3ar,7ac)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione (73839-58-4)

Guidance literature:

at 190 ℃;

DOI:10.1021/jo01364a014

upstream raw materials:

3-(N-methylpiperazino)propylamine

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

1-methyl-piperazine

3-(4-methylpiperazin-1-yl)propanenitrile

Downstream raw materials:

2-[3-(4-methyl-piperazino)-propyl]-(3ar,7ac)-2,3,3a,4,7,7a-hexahydro-1H-isoindole