N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide

Base Information

Chemical Name:N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide
CAS No.:90235-58-8
Molecular Formula:C₁₆H₁₈N₂O
Molecular Weight:254.332
Hs Code.:
DSSTox Substance ID:DTXSID50530448

Synonyms:90235-58-8;DTXSID50530448;N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide

Suppliers and Price of N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:254.141913202
Heavy Atom Count:19
Complexity:441

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NC(=O)C#CC#CN(C)C1=CC=CC=C1

Technology Process of N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide

There total 3 articles about N-tert-Butyl-5-[methyl(phenyl)amino]penta-2,4-diynamide 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: 44.0%

: 350244-59-6
C₁₁H₈LiN

: 1609-86-5
Tert-butyl isocyanate

: 90235-58-8
N-tert-Butyl-5-(methylphenylamino)-2,4-pentadiinamid

Guidance literature:: In diethyl ether; at 0 ℃; for 2h;

Reference yield:

: 82505-76-8
(3,4,4-Trichloro-N-methyl-N-phenyl-3-buten-1-inyl)amin

: 90235-58-8
N-tert-Butyl-5-(methylphenylamino)-2,4-pentadiinamid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.6 N LiBu / diethyl ether; hexane / 1.5 h / Ambient temperature

2: 44 percent / diethyl ether / 2 h / 0 °C

With n-butyllithium; In diethyl ether; hexane;

Reference yield:

: 35954-01-9
lithium N-methylanilide

: 90235-58-8
N-tert-Butyl-5-(methylphenylamino)-2,4-pentadiinamid

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent

2: 1.6 N LiBu / diethyl ether; hexane / 1.5 h / Ambient temperature

3: 44 percent / diethyl ether / 2 h / 0 °C

With n-butyllithium; In diethyl ether; hexane;