N-methylcyclopropanamine

Base Information

• Chemical Name: N-methylcyclopropanamine
• CAS No.: 5163-20-2
• Molecular Formula: C4H9N
• Molecular Weight: 71.1222
• European Community (EC) Number: 815-248-2
• DSSTox Substance ID: DTXSID20452406
• Nikkaji Number: J1.598.917C
• Wikidata: Q72489788
• Mol file: 5163-20-2.mol

Synonyms:N-methylcyclopropanamine;5163-20-2;Cyclopropyl-methyl-amine;N-CYCLOPROPYLMETHYLAMINE;Cyclopropanamine, N-methyl-;methylcyclopropylamine;N-METHYL-CYCLOPROPANAMINE;cyclopropyl methyl amine;dimethylenemethylamine;cyclopropyl methylamine;Cyclopropyl-methylamine;N-methylcyclopropylamine;N-cyclopropyl-methylamine;N-methyl cyclopropylamine;N-methyl cyclopropyl amine;N-cyclopropyl-N-methylamine;n-methyl-n-cyclopropyl-amine;DTXSID20452406;VEBLEROFGPOMPB-UHFFFAOYSA-N;MFCD00045391;AKOS000160824;SB20428;AM20100262;FT-0685242;EN300-39986;Z138412880

Chemical Property of N-methylcyclopropanamine

Chemical Property:

• Vapor Pressure: 147.685mmHg at 25°C
• Refractive Index: 1.443
• Boiling Point: 67.085 °C at 760 mmHg
• PKA: 9.46±0.20(Predicted)
• Flash Point: -34.796 °C
• PSA: 12.03000
• Density: 0.851 g/cm³
• LogP: 0.75910
• XLogP3: 0.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 71.073499291
• Heavy Atom Count: 5
• Complexity: 30.6

Purity/Quality:

99% ^*data from raw suppliers

n-Methylcyclopropanamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC1CC1

Refernces

Rapid assessment of a novel series of selective CB₂ agonists using parallel synthesis protocols: A Lipophilic Efficiency (LipE) analysis

10.1016/j.bmcl.2009.05.062

The study focuses on the rapid assessment and synthesis of a novel series of selective CB2 agonists, which are compounds that activate the CB2 receptor, a target for pain treatment. The researchers designed a series of libraries based on the 1-(cyclopropylmethyl)-2-alkyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-5-ium templates and sulfonamide derivatives. These compounds were synthesized to evaluate their in vitro potency and metabolic stability, with the aim of developing potent, metabolically stable CB2 agonists. The study also analyzed the Lipophilic Efficiency (LipE) of potent compounds to gain insights for the design of more effective CB2 agonists. The chemicals used in the study included various alkyl, carbamate, urea, amide, and sulfonamide derivatives, as well as reagents like cyclopropyl methyl amine, Pd/C, PtO2, and various acids, amines, and alcohols for the synthesis and functionalization of the scaffolds. The purpose of these chemicals was to create a diverse set of compounds that could be tested for their ability to activate the CB2 receptor selectively, with the goal of improving pain treatment options while avoiding psychotropic side-effects associated with CB1 receptor activation.

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