Benzeneethanamine, N-methyl-N-2-propynyl-

Base Information

Chemical Name:Benzeneethanamine, N-methyl-N-2-propynyl-
CAS No.:2322-02-3
Molecular Formula:C12H15N
Molecular Weight:173.258
Hs Code.:
DSSTox Substance ID:DTXSID30434091
Nikkaji Number:J269.499I

Synonyms:MPPE;Benzeneethanamine, N-methyl-N-2-propynyl-;SCHEMBL1176965;DTXSID30434091;N-methyl-N-propargyl-2-phenylethylamine;2322-02-3

Suppliers and Price of Benzeneethanamine, N-methyl-N-2-propynyl-

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

Total 1 raw suppliers

Chemical Property of Benzeneethanamine, N-methyl-N-2-propynyl-

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:173.120449483
Heavy Atom Count:13
Complexity:171

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CCC1=CC=CC=C1)CC#C

Technology Process of Benzeneethanamine, N-methyl-N-2-propynyl-

There total 5 articles about Benzeneethanamine, N-methyl-N-2-propynyl- 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: 75.0%

: 106-96-7
propargyl bromide

: 589-08-2
N-Methyl-N-phenethylamine

: 2322-02-3
C₁₂H₁₅N

Guidance literature:: With potassium carbonate; In tetrahydrofuran; Reflux;
DOI:10.1021/cc100029y

Reference yield: 52.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 58185-47-0
N-phenethyl-N-prop-2-ynylamine

: 2322-02-3
C₁₂H₁₅N

Guidance literature:: With formic acid; for 4h; Reflux;
DOI:10.1002/chem.202101824

Reference yield:

: 2-nitro-N-phenethyl-N-(prop-2-yn-1-yl)benzenesulfonamide

: 2322-02-3
C₁₂H₁₅N

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; thiophenol / acetonitrile / 8 h / 75 °C

2: formic acid / 4 h / Reflux

With formic acid; potassium carbonate; thiophenol; In acetonitrile;
DOI:10.1002/chem.202101824