N-(2-aminoethyl)-N-methylcyclopropanamine

Base Information

Chemical Name:N-(2-aminoethyl)-N-methylcyclopropanamine
CAS No.:126105-24-6
Molecular Formula:C₆H₁₄N₂
Molecular Weight:114.191
Hs Code.:
European Community (EC) Number:856-693-2

Synonyms:N-(2-aminoethyl)-N-methylcyclopropanamine;126105-24-6;N'-cyclopropyl-N'-methylethane-1,2-diamine;SCHEMBL3429977;BOGOVRPYKWYEKM-UHFFFAOYSA-N;N-methyl-N-cyclopropylethylenediamine;AKOS009416770;AT25788;CS-0251428;EN300-54723;N(1)-cyclopropyl-N(1)-methyl-ethane-1,2-diamine;N1-CYCLOPROPYL-N1-METHYLETHANE-1,2-DIAMINE;F2187-0486

Suppliers and Price of N-(2-aminoethyl)-N-methylcyclopropanamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N-(2-aminoethyl)-N-methylcyclopropanamine
100mg
$ 240.00

American Custom Chemicals Corporation
N-(2-AMINOETHYL)-N-METHYLCYCLOPROPANAMINE 95.00%
5G
$ 1928.08

American Custom Chemicals Corporation
N-(2-AMINOETHYL)-N-METHYLCYCLOPROPANAMINE 95.00%
2.5G
$ 1473.14

American Custom Chemicals Corporation
N-(2-AMINOETHYL)-N-METHYLCYCLOPROPANAMINE 95.00%
1G
$ 983.52

AK Scientific
N-(2-Aminoethyl)-N-methylcyclopropanamine
250mg
$ 340.00

AK Scientific
N-(2-Aminoethyl)-N-methylcyclopropanamine
100mg
$ 268.00

Total 3 raw suppliers

Chemical Property of N-(2-aminoethyl)-N-methylcyclopropanamine

Chemical Property:

XLogP3:-0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:114.115698455
Heavy Atom Count:8
Complexity:68.9

Purity/Quality:

99% ^*data from raw suppliers

N-(2-aminoethyl)-N-methylcyclopropanamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(CCN)C1CC1

Technology Process of N-(2-aminoethyl)-N-methylcyclopropanamine

There total 4 articles about N-(2-aminoethyl)-N-methylcyclopropanamine 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: 88.0%

: 126105-23-5
N-acetyl-N'-cyclopropyl-N'-methylethylenediamine

: 126105-24-6
N-cyclopropyl-N-methylethylenediamine

Guidance literature:: With hydrogenchloride; for 2h; Heating;
DOI:10.1016/0223-5234(93)90129-3

Reference yield:

: 91907-31-2
N-benzyl-N-cyclopropylethylenediamine

: 126105-24-6
N-cyclopropyl-N-methylethylenediamine

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / 0.5 h / 50 - 70 °C

2: 100 percent / H₂, HCl / 5percent Pd/C / ethanol / 2 h / Ambient temperature

3: 91 percent / potassium carbonate / dimethylformamide / 0.25 h / 80 °C

4: 88 percent / 15percent aq. HCl / 2 h / Heating

With hydrogenchloride; hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(93)90129-3

Reference yield:

: 126105-21-3
N-acetyl-N'benzyl-N'-cyclopropylethylenediamine

: 126105-24-6
N-cyclopropyl-N-methylethylenediamine

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / H₂, HCl / 5percent Pd/C / ethanol / 2 h / Ambient temperature

2: 91 percent / potassium carbonate / dimethylformamide / 0.25 h / 80 °C

3: 88 percent / 15percent aq. HCl / 2 h / Heating

With hydrogenchloride; hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(93)90129-3