Piritramide

Base Information

• Chemical Name: Piritramide
• CAS No.: 302-41-0
• Molecular Formula: C27H34N4O
• Molecular Weight: 430.593
• European Community (EC) Number: 206-124-3
• UNII: 4RP92LYZ2F
• DSSTox Substance ID: DTXSID00184293
• Nikkaji Number: J5.481J
• Wikipedia: Piritramide
• Wikidata: Q416439
• NCI Thesaurus Code: C119750
• Metabolomics Workbench ID: 49677
• ChEMBL ID: CHEMBL559288
• Mol file: 302-41-0.mol

Synonyms:Dipidolor;Dipydolor;Pirinitramide;Piritramid;Piritramide

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Chemical Property of Piritramide

Chemical Property:

• Vapor Pressure: 2.13E-16mmHg at 25°C
• Melting Point: 149-150°
• Refractive Index: 1.59
• Boiling Point: 642.5 °C at 760 mmHg
• PKA: 16.19±0.20(Predicted)
• Flash Point: 342.3 °C
• PSA: 73.36000
• Density: 1.15 g/cm³
• LogP: 4.26828
• Storage Temp.: Controlled Substance, -20°C Freezer
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 430.27326172
• Heavy Atom Count: 32
• Complexity: 638

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(CC1)C2(CCN(CC2)CCC(C#N)(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)N
• Recent ClinicalTrials: Influence of Opioid Analgesia on Circulating Tumor Cells in Open Colorectal Cancer Surgery
• Recent EU Clinical Trials: Post-operative patient controlled intravenous oxyco-done vs patient controlled intrav nous piritramide. A randomized controlled trial.
• Uses: Piritramide is a synthetic opioid commonly used in Germany and Austria for the analgesia of pediatric patients.
• Therapeutic Function: Analgesic

Technology Process of Piritramide

There total 1 articles about Piritramide 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:

→ pirinitramide (302-41-0)

Guidance literature:

4-Piperidino-4-piperidincarboxamid, 3-Cyano-3,3-diphenylpropylhalid, Na2CO3, Methylisobutylketon;

DOI:10.1021/jm00335a010

Refernces