4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one

Base Information

• Chemical Name: 4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one
• CAS No.: 64693-19-2
• Molecular Formula: C₁₅H₁₆N₂O
• Molecular Weight: 240.305
• Hs Code.: 2925290090
• European Community (EC) Number: 684-748-9
• NSC Number: 401162,14727
• Nikkaji Number: J75.336J
• ChEMBL ID: CHEMBL3276919
• Mol file: 64693-19-2.mol

Synonyms:64693-19-2;4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one;WLN: L6V DYJ B1 DUNR DN1&1;2, 4-(p-dimethylaminophenyl)imino-2-methyl-;2, 4-[[4-(dimethylamino)phenyl]imino]-2-methyl-;NSC 14727;BRN 2376942;NSC14727;2,5-Cyclohexadien-1-one, 4-(p-dimethylaminophenyl)imino-2-methyl-;SCHEMBL2680700;CHEMBL3276919;4-[(p-Dimethylaminophenyl)imino]-2-methyl-2,5-cyclohexadien-1-one;NSC-14727;NSC401162;AKOS024340670;NSC-401162;4-(4-(DIMETHYLAMINO)PHENYLIMINO)-2-METHYL-2,5-CYCLOHEXADIEN-1-ONE

Chemical Property of 4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one

Chemical Property:

• Vapor Pressure: 1.03E-05mmHg at 25°C
• Boiling Point: 371.5°Cat760mmHg
• Flash Point: 178.5°C
• PSA: 32.67000
• Density: 1.05g/cm³
• LogP: 2.91030
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 240.126263138
• Heavy Atom Count: 18
• Complexity: 410

Purity/Quality:

99% ^*data from raw suppliers

4-(4-(DIMETHYLAMINO)PHENYLIMINO)-2-METHYL-2,5-CYCLOHEXADIEN-1-ONE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=NC2=CC=C(C=C2)N(C)C)C=CC1=O

Technology Process of 4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one

There total 5 articles about 4-(p-Dimethylaminophenyl)imino-2-methyl-2,5-cyclohexadiene-1-one 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:

4-dimethylaminophenylamine dihydrochloride (536-46-9,13806-04-7) + ortho-cresol (95-48-7,77504-84-8) → methyl-[1,4]benzoquinone-4-(4-dimethylamino-phenylimine) (64693-19-2)

Guidance literature:

With alkaline aqueous sodium hypochlorite; sodium acetate;

DOI:10.1021/ja01871a043

Reference yield:

N,N-dimethyl-p-phenylenediamine hydrochloride (2052-46-2,13806-04-7) + ortho-cresol (95-48-7,77504-84-8) → methyl-[1,4]benzoquinone-4-(4-dimethylamino-phenylimine) (64693-19-2)

Guidance literature:

With sodium carbonate; silver(I) chloride; In ethanol;

DOI:10.1021/jm00199a003

Reference yield:

2-methyl-4-chlorophenol (1570-64-5) + 4-dimethylaminophenylamine dihydrochloride (536-46-9,13806-04-7) → methyl-[1,4]benzoquinone-4-(4-dimethylamino-phenylimine) (64693-19-2)

Guidance literature:

With ethanol; sodium carbonate; silver(I) chloride;

DOI:10.1021/ja01175a004

upstream raw materials:

2-methyl-4-chlorophenol

4-dimethylaminophenylamine dihydrochloride

ortho-cresol

N,N-dimethyl-p-phenylenediamine hydrochloride

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