(E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine

Base Information

Chemical Name:(E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine
CAS No.:67411-28-3
Molecular Formula:C11H13NO
Molecular Weight:175.23
Hs Code.:
DSSTox Substance ID:DTXSID80496947

Synonyms:(E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine;67411-28-3;benzylidene-b-vinyloxyethylamine;DTXSID80496947;N-benzylidene-2-(vinyloxy)ethylamine

Suppliers and Price of (E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine

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 3 raw suppliers

Chemical Property of (E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:175.099714038
Heavy Atom Count:13
Complexity:160

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=COCCN=CC1=CC=CC=C1

Technology Process of (E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine

There total 1 articles about (E)-N-[2-(Ethenyloxy)ethyl]-1-phenylmethanimine 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:

: 7336-29-0
2-aminoethyl vinyl ether

: 100-52-7
benzaldehyde

: 67411-28-3
benzylidene-β-vinyloxyethylamine

Guidance literature:: In toluene;
DOI:10.1007/BF00929034

Reference yield: 92.0%

: 67411-28-3
benzylidene-β-vinyloxyethylamine

: 73731-97-2
N-benzyl-β-vinyloxyethylamine

Guidance literature:: With sodium tetrahydroborate; In methanol; at 45 - 50 ℃; for 1h; Product distribution; reduction of vinyl ethers of imino alcohols;
DOI:10.1007/BF00951887