gamma,gamma-Dimethyl-N-phenylbenzenebutanamide

Base Information

• Chemical Name: gamma,gamma-Dimethyl-N-phenylbenzenebutanamide
• CAS No.: 4408-56-4
• Molecular Formula: C₁₈H₂₁NO
• Molecular Weight: 267.371
• DSSTox Substance ID: DTXSID901283335
• Mol file: 4408-56-4.mol

Synonyms:DTXSID901283335;AKOS000276925;4408-56-4;I(3),I(3)-Dimethyl-N-phenylbenzenebutanamide

Chemical Property of gamma,gamma-Dimethyl-N-phenylbenzenebutanamide

Chemical Property:

• XLogP3: 4.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 267.162314293
• Heavy Atom Count: 20
• Complexity: 299

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)(CCC(=O)NC1=CC=CC=C1)C2=CC=CC=C2

Technology Process of gamma,gamma-Dimethyl-N-phenylbenzenebutanamide

There total 3 articles about gamma,gamma-Dimethyl-N-phenylbenzenebutanamide 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:

dihydro-5,5-dimethyl-2(3H)-furanone (3123-97-5) → 4-methyl-4-phenyl-valeric acid anilide (4408-56-4)

Guidance literature:

Multi-step reaction with 2 steps

1: aluminium bromide

2: 200 °C

With aluminum tri-bromide;

Reference yield:

benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → 4-methyl-4-phenyl-valeric acid anilide (4408-56-4)

Guidance literature:

Multi-step reaction with 2 steps

1: aluminium bromide

2: 200 °C

With aluminum tri-bromide;

Reference yield:

4-methyl-4-phenylpentanoic acid (4408-55-3) + aniline (62-53-3) → 4-methyl-4-phenyl-valeric acid anilide (4408-56-4)

Guidance literature:

at 200 ℃;

upstream raw materials:

4-methyl-4-phenylpentanoic acid

aniline

dihydro-5,5-dimethyl-2(3H)-furanone

benzene