(2E)-N-Phenylpentan-2-imine

Base Information

Chemical Name:(2E)-N-Phenylpentan-2-imine
CAS No.:57711-63-4
Molecular Formula:C11H15N
Molecular Weight:161.247
Hs Code.:
DSSTox Substance ID:DTXSID90506622
Nikkaji Number:J1.586.755H

Synonyms:57711-63-4;(2E)-N-Phenylpentan-2-imine;SCHEMBL5799996;SCHEMBL18947275;DTXSID90506622

Suppliers and Price of (2E)-N-Phenylpentan-2-imine

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
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price

Total 0 raw suppliers

Chemical Property of (2E)-N-Phenylpentan-2-imine

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:161.120449483
Heavy Atom Count:12
Complexity:143

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(=NC1=CC=CC=C1)C

Technology Process of (2E)-N-Phenylpentan-2-imine

There total 4 articles about (2E)-N-Phenylpentan-2-imine 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: 55.0%

: 627-19-0
1-Pentyne

: 62-53-3
aniline

: 57711-63-4
N-(1-methylbutylidene)aniline

Guidance literature:: With mercury dichloride; In tetrahydrofuran; for 6h; Ambient temperature;

Reference yield: 34.0%

: 62-53-3
aniline

: 693-02-7
hex-1-yne

: 57711-63-4
N-(1-methylbutylidene)aniline

: C₁₈H₂₇N

Guidance literature:: With tetrafluoroboric acid diethyl ether; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; In toluene; at 100 ℃; for 24h; Inert atmosphere; Schlenk technique;
DOI:10.1021/om501253v