N-Benzyl-2-(1H-imidazol-1-yl)ethanamine

Base Information

Chemical Name:N-Benzyl-2-(1H-imidazol-1-yl)ethanamine
CAS No.:151642-11-4
Molecular Formula:C₁₂H₁₅N₃
Molecular Weight:201.271
Hs Code.:
ChEMBL ID:CHEMBL561603
DSSTox Substance ID:DTXSID60595826
Wikidata:Q82490919

Synonyms:151642-11-4;N-Benzyl-2-(1H-imidazol-1-yl)ethanamine;N-Benzyl-2-(1H-imidazol-1-yl)ethan-1-amine;benzyl[2-(1H-imidazol-1-yl)ethyl]amine;CHEMBL561603;SCHEMBL6638645;DTXSID60595826;BGA64211;N-benzyl-2-imidazol-1-ylethanamine;N-benzyl-2-imidazol-1-yl-ethanamine;AKOS008992480

Suppliers and Price of N-Benzyl-2-(1H-imidazol-1-yl)ethanamine

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

Crysdot
N-Benzyl-2-(1H-imidazol-1-yl)ethanamine 95+%
5g
$ 746.00

Chemenu
N-benzyl-2-(1H-imidazol-1-yl)ethan-1-amine 95%
5g
$ 704.00

Alichem
N-Benzyl-2-(1H-imidazol-1-yl)ethanamine
1g
$ 400.00

Total 2 raw suppliers

Chemical Property of N-Benzyl-2-(1H-imidazol-1-yl)ethanamine

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:201.126597491
Heavy Atom Count:15
Complexity:166

Purity/Quality:

95+% ^*data from raw suppliers

N-Benzyl-2-(1H-imidazol-1-yl)ethanamine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNCCN2C=CN=C2

Technology Process of N-Benzyl-2-(1H-imidazol-1-yl)ethanamine

There total 4 articles about N-Benzyl-2-(1H-imidazol-1-yl)ethanamine 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:

: 288-32-4
1H-imidazole

: 65894-26-0
N-benzyl-2-bromoethylamine

: 151642-11-4
1-(2-benzylaminoethyl)-1H-imidazole

Guidance literature:: In acetonitrile; for 8h; Reflux;

Reference yield:

: 100-44-7
benzyl chloride

: 151642-11-4
1-(2-benzylaminoethyl)-1H-imidazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 8 h / 20 °C / Cooling with ice

2: acetonitrile / 8 h / Reflux

With triethylamine; In dichloromethane; acetonitrile;

Reference yield:

: 100-39-0
benzyl bromide

: 151642-11-4
1-(2-benzylaminoethyl)-1H-imidazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 5 h / 20 °C / Cooling with ice

2: acetonitrile / 8 h / Reflux

With triethylamine; In dichloromethane; acetonitrile;