N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide

Base Information

Chemical Name:N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide
CAS No.:103708-90-3
Molecular Formula:C₁₆H₂₃NO
Molecular Weight:245.365
Hs Code.:
DSSTox Substance ID:DTXSID20544931
Mol file:103708-90-3.mol

Synonyms:103708-90-3;N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide;DTXSID20544931

Suppliers and Price of N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide

Supply Marketing:

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

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Chemical Property of N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:245.177964357
Heavy Atom Count:18
Complexity:306

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide

There total 2 articles about N-(2,2,4,4-Tetramethylpentan-3-ylidene)benzamide 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: 67.0%

: 29097-52-7
2,2,4,4-tetramethyl-3-pentanone imine

: 98-88-4
benzoyl chloride

: 103708-90-3
N-(1-tert-Butyl-2,2-dimethylpropyliden)benzamid

Guidance literature:: With triethylamine; In toluene; for 14h; Ambient temperature;

Reference yield:

: 630-18-2
tert-butyl isocyanide

: 594-19-4
tert.-butyl lithium

: N-[1-Ethoxy-2,2-dimethyl-prop-(E)-ylidene]-benzamide

: 103708-90-3
N-(1-tert-Butyl-2,2-dimethylpropyliden)benzamid

: 2,2,4-Tri-tert-butyl-6-phenyl-2H-1,3,5-oxadiazin

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given; 1) diethyl ether, n-pentane, room temperature, 30 min.; 2) diethyl ether, room temperature, 36 h;