Mefenorex

Base Information

• Chemical Name: Mefenorex
• CAS No.: 17243-57-1
• Deprecated CAS: 24954-70-9
• Molecular Formula: C₁₂H₁₈ClN
• Molecular Weight: 211.735
• European Community (EC) Number: 241-279-0
• UNII: 7FT4O2NC8G,K98M4N387W,85052999IT
• DSSTox Substance ID: DTXSID6057665
• Nikkaji Number: J9.089A
• Wikipedia: Mefenorex
• Wikidata: Q10579342
• NCI Thesaurus Code: C83915
• Metabolomics Workbench ID: 154630
• ChEMBL ID: CHEMBL2110962
• Mol file: 17243-57-1.mol

Synonyms:chloropropylamphetamine;Incital;mefenorex;mefenorex hydrochloride;mefenorex, (+-)-isomer;Pondinil;Ro 4-5282

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of Mefenorex

Chemical Property:

• Vapor Pressure: 0.000841mmHg at 25°C
• Boiling Point: 305.1°Cat760mmHg
• PKA: 9.67±0.28(Predicted)
• Flash Point: 138.3°C
• PSA: 12.03000
• Density: 1.013g/cm³
• LogP: 3.22700
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 211.1127773
• Heavy Atom Count: 14
• Complexity: 132

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CC1=CC=CC=C1)NCCCCl
• Uses: Anorexic.
• Therapeutic Function: Anorexic

Technology Process of Mefenorex

There total 1 articles about Mefenorex 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:

→ (±)-3-chloro-N-(1-methyl-2-phenylethyl)propan-1-amine (17243-57-1,111051-41-3,111051-42-4)

Guidance literature:

a) Ph-CH2-CH(NH2)-CH3, OCH-CH2-CH2Cl, H2/PtO2;

Reference yield:

(±)-3-chloro-N-(1-methyl-2-phenylethyl)propan-1-amine (17243-57-1,111051-41-3,111051-42-4) → C12H18ClN + C12H18ClN

Guidance literature:

With β‐cyclodextrin; In aq. phosphate buffer; at 25 ℃; pH=2.5; Reagent/catalyst; Resolution of racemate;

DOI:10.1002/chir.23268