Benzenamine, 4-[2-(4-quinolinyl)ethenyl]-

Base Information

• Chemical Name: Benzenamine, 4-[2-(4-quinolinyl)ethenyl]-
• CAS No.: 54-00-2
• Molecular Formula: C17H14N2
• Molecular Weight: 246.3065
• NSC Number: 59065
• ChEMBL ID: CHEMBL1986365
• Mol file: 54-00-2.mol

Synonyms:54-00-2;4-p-Diaminostyrylquinone;Benzenamine, 4-[2-(4-quinolinyl)ethenyl]-;NSC59065;4-(2-(Quinolin-4-yl)vinyl)aniline;4-[(E)-2-quinolin-4-ylethenyl]aniline;4-[2-(4-quinolinyl)vinyl]phenylamine;Quinoline, 4-(4-aminostyryl);CHEMBL1986365;Quinoline, 4-(p-aminostyryl)-;4-(4-amino-trans-styryl)quinoline;NSC-59065;4-[(E)-2-(4-quinolyl)vinyl]aniline;NCGC00184051-01;NCGC00184051-02;NCGC00184051-03;NCGC00184051-04;NCGC00184051-05;NCGC00184051-06;NCGC00184051-07;NCGC00184051-08;NCGC00184051-09;NCGC00184051-10;NCGC00184051-11;NCGC00184051-12;NCGC00184051-13;NCGC00184051-14;NCGC00184051-15;NCGC00184051-16;NCGC00184051-17;NCGC00184051-18;NCGC00184051-19;NCGC00184051-20;AT-051/43421260;Z3965387614

Chemical Property of Benzenamine, 4-[2-(4-quinolinyl)ethenyl]-

Chemical Property:

• Vapor Pressure: 6.29E-09mmHg at 25°C
• Boiling Point: 467.9°C at 760 mmHg
• Flash Point: 267.9°C
• Density: 1.217g/cm³
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 246.115698455
• Heavy Atom Count: 19
• Complexity: 304

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=CC=N2)C=CC3=CC=C(C=C3)N
• Isomeric SMILES: C1=CC=C2C(=C1)C(=CC=N2)/C=C/C3=CC=C(C=C3)N

Technology Process of Benzenamine, 4-[2-(4-quinolinyl)ethenyl]-

There total 3 articles about Benzenamine, 4-[2-(4-quinolinyl)ethenyl]- 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: 77.0%

→ 4-(4'-aminostyryl)quinoline (54-00-2)

Guidance literature:

Reference yield:

C6H4NCH2CHCCH2 (491-35-0) + para-acetamidobenzaldehyde (122-85-0) → 4-(4-amino-trans-styryl)quinoline (54-00-2)

Guidance literature:

With zinc(II) chloride; at 180 ℃;

DOI:10.1021/jo01101a610

Reference yield:

4-(4-nitro-trans-styryl)quinoline (40317-02-0,4594-97-2) → 4-(4-amino-trans-styryl)quinoline (54-00-2)

Guidance literature:

With hydrogenchloride; tin(ll) chloride;

DOI:10.1021/jo01101a610

upstream raw materials:

C₆H₄NCH₂CHCCH₂

para-acetamidobenzaldehyde

4-(4-nitro-trans-styryl)quinoline

Downstream raw materials:

4-(4-azido-trans-styryl)quinoline

4-(trans-2-[4]quinolyl-vinyl)-N-(4-dimethylamino-benzyliden)-aniline

[4-(trans-2-[4]quinolyl-vinyl)-phenyl]-carbamic acid ethyl ester

[4-(trans-2-[4]quinolyl-vinyl)-phenyl]-urea

Refernces