Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-

Base Information

Chemical Name:Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-
CAS No.:88152-00-5
Molecular Formula:C24H20N6O2S
Molecular Weight:456.5196
Hs Code.:
DSSTox Substance ID:DTXSID10236858
Wikidata:Q83118945

Synonyms:88152-00-5;BRN 4607180;Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-;2-Phenyl-3-(4-(pyrimidin-2-yl-aminosulfonyl)phenylhydrazino)indole;4-(2-(2-Phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinylbenzenesulfonamide;4-[2-(2-Phenyl-1H-indol-3-yl)hydrazino]-N-(2-pyrimidinyl)benzenesulfonamide;C24H20N6O2S;DTXSID10236858;LS-31701

Suppliers and Price of Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-

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 0 raw suppliers

Chemical Property of Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-

Chemical Property:

Vapor Pressure:4.31E-18mmHg at 25°C
Boiling Point:675.2°C at 760 mmHg
Flash Point:362.2°C
Density:1.474g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:456.13684508
Heavy Atom Count:33
Complexity:711

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=C(C3=CC=CC=C3N2)NNC4=CC=C(C=C4)S(=O)(=O)NC5=NC=CC=N5

Technology Process of Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl-

There total 3 articles about Benzenesulfonamide, 4-(2-(2-phenyl-1H-indol-3-yl)hydrazino)-N-2-pyrimidinyl- 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: 65.0%

: 88151-91-1
2-Phenyl-3-<4-(pyrimidin-2-yl-aminosulphonyl)phenylazo>indole

: 88152-00-5
2-Phenyl-3-<4-(pyrimidin-2-yl-aminosulphonyl)phenylhydrazino>indole

Guidance literature:: With hydrazine hydrate; nickel; In ethanol; for 4h; Heating;

Reference yield:

: 948-65-2
2-phenyl-indole

: 88152-00-5
2-Phenyl-3-<4-(pyrimidin-2-yl-aminosulphonyl)phenylhydrazino>indole

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridine / 1) cooled in ice, 1 h 2) room temperature, 1 h 3) reflux, 4 h

2: 65 percent / Hydrazine hydrate / Raney-Ni / ethanol / 4 h / Heating

With hydrazine hydrate; nickel; In pyridine; ethanol;

Reference yield:

: 131430-29-0
C₁₀H₈ClN₅O₂S

: 88152-00-5
2-Phenyl-3-<4-(pyrimidin-2-yl-aminosulphonyl)phenylhydrazino>indole

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridine / 1) cooled in ice, 1 h 2) room temperature, 1 h 3) reflux, 4 h

2: 65 percent / Hydrazine hydrate / Raney-Ni / ethanol / 4 h / Heating

With hydrazine hydrate; nickel; In pyridine; ethanol;