N-methylcyclopentanamine

Base Information

• Chemical Name: N-methylcyclopentanamine
• CAS No.: 2439-56-7
• Molecular Formula: C6H13 N
• Molecular Weight: 99.1759
• Hs Code.: 2921300090
• European Community (EC) Number: 675-202-0
• DSSTox Substance ID: DTXSID50427268
• Nikkaji Number: J994.195I
• Mol file: 2439-56-7.mol

Synonyms:N-methylcyclopentanamine;2439-56-7;Cyclopentyl-methyl-amine;N-METHYLCYCLOPENTYLAMINE;N-cyclopentyl-N-methylamine;Cyclopentanamine, N-methyl-;N-cyclopentyl-N-methyl amine;MFCD00019277;Cyclopentanamine,N-methyl-;methylcyclopentylamine;cycloamyl-methyl-amine;cyclopentyl-methylamine;N-methyl cyclopentanamine;N-Methyl-cyclopentylamine;N-(cyclopentyl)-methylamine;F2184-0196;DTXSID50427268;HMS1773O08;cyclopentyl-methyl-amine, AldrichCPR;AKOS000264144;CCG-358843;BB 0218283;FT-0683160;EC-000.2044;EN300-23728;A817269;Z102766802

Chemical Property of N-methylcyclopentanamine

Chemical Property:

• Vapor Pressure: 15.8mmHg at 25°C
• Boiling Point: 119.7°Cat760mmHg
• PKA: 10.94±0.20(Predicted)
• Flash Point: 6.9°C
• PSA: 12.03000
• Density: 0.84g/cm³
• LogP: 1.53930
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 99.104799419
• Heavy Atom Count: 7
• Complexity: 46.1

Purity/Quality:

99%, ^*data from raw suppliers

Cyclopentylmethylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 22-37/38-41-52
• Safety Statements: 26-39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC1CCCC1

Technology Process of N-methylcyclopentanamine

There total 1 articles about N-methylcyclopentanamine 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:

cyclopentanone (120-92-3) + methylamine (74-89-5) → N-methylcyclopentylamine (2439-56-7) + Cyclopentanol (96-41-3)

Guidance literature:

With potassium hydroxide; potassium phosphate; In water; at 18 - 20 ℃; pH 12, electrochemical reaction;

Reference yield: 91.0%

N-methylcyclopentylamine (2439-56-7) + 4-Bromo-1-fluoro-2-nitrobenzene (364-73-8) → 4-bromo-N-cyclopentyl-N-methyl-2-nitroaniline

Guidance literature:

In tetrahydrofuran; at 20 - 60 ℃;

Reference yield: 84.0%

N-methylcyclopentylamine (2439-56-7) + 3-((3,4-difluorophenyl)carbamoyl)-4-fluorobenzene-1-sulfonyl chloride (1616809-39-2) → 5-(N-cyclopentyl-N-methylsulfamoyl)-N-(3,4-difluorophenyl)-2-fluorobenzamide

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;

DOI:10.1016/j.ejmech.2017.06.062

upstream raw materials:

cyclopentanone

methylamine

Downstream raw materials:

2,4-Dibromo-6-[(cyclopentyl-methyl-amino)-methyl]-phenol

N³-Cyclopentyl-N³-methyl-2,4-dinitro-6-trifluoromethyl-benzene-1,3-diamine

Rifamycin-B-(cyclopentyl-methyl-amid)

C₁₄H₂₁N₃

Refernces