N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide

Base Information

Chemical Name:N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide
CAS No.:23305-70-6
Molecular Formula:C38H30 N8
Molecular Weight:598.71
Hs Code.:
NSC Number:242017
DSSTox Substance ID:DTXSID70422179
Mol file:23305-70-6.mol

Synonyms:NSC242017;23305-70-6;DTXSID70422179;21520-87-6;NSC-242017

Suppliers and Price of N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide

Chemical Property:

Boiling Point:748.7°Cat760mmHg
Flash Point:406.6°C
Density:1.17g/cm³
XLogP3:11.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:598.25934299
Heavy Atom Count:46
Complexity:902

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=NNC2=CC=CC=C2)N=NC3=CC=C(C=C3)C4=CC=C(C=C4)N=NC(=NNC5=CC=CC=C5)C6=CC=CC=C6
Isomeric SMILES:C1=CC=C(C=C1)/C(=N\NC2=CC=CC=C2)/N=NC3=CC=C(C=C3)C4=CC=C(C=C4)N=N/C(=N/NC5=CC=CC=C5)/C6=CC=CC=C6

Technology Process of N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide

There total 4 articles about N'-anilino-N-[4-[4-[[(E)-N-anilino-C-phenylcarbonimidoyl]diazenyl]phenyl]phenyl]iminobenzenecarboximidamide 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: 58.8%

: 92-87-5
p,p'-diaminobiphenyl

: 588-64-7
benzaldehyde phenylhydrazone

: 23305-70-6
1,1′-([1,1′-biphenyl]-4,4′-diyl)bis(3,5-diphenylformazan)

Guidance literature:: p,p'-diaminobiphenyl; With hydrogenchloride; sodium nitrite; In water;

benzaldehyde phenylhydrazone; With sodium hydroxide; In methanol; water; at 0 - 5 ℃; for 27h;
DOI:10.1134/S1070428021100055

Reference yield:

: 100-52-7
benzaldehyde

: 23305-70-6
1,1′-([1,1′-biphenyl]-4,4′-diyl)bis(3,5-diphenylformazan)

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium acetate / 1,4-dioxane; water / 20 °C

2.1: sodium nitrite; hydrogenchloride / water

2.2: 27 h / 0 - 5 °C

With hydrogenchloride; sodium acetate; sodium nitrite; In 1,4-dioxane; water;
DOI:10.1134/S1070428021100055