7472-70-0

Basic information

• Product Name: 1,2-dichloro-N,N-bis(4-methylphenyl)ethane-1,2-diimine
• CAS NO: 7472-70-0
• Molecular Formula: C₁₆H₁₄Cl₂N₂
• Molecular Weight: 305.207
• Mol File: 7472-70-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,2-dichloro-N,N-bis(4-methylphenyl)ethane-1,2-diimine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dichloro-N,N-bis(4-methylphenyl)ethane-1,2-diimine(7472-70-0)
• EPA Substance Registry System: 1,2-dichloro-N,N-bis(4-methylphenyl)ethane-1,2-diimine(7472-70-0)

Safety Data

• Hazardous Substances Data: 7472-70-0(Hazardous Substances Data)

Usage

Type of Compound

Synthetic compound

Use

Antimalarial medication

Mechanism of Action

Interferes with the metabolism of the malaria parasite, preventing its growth and spread in the body

Effectiveness

Particularly effective in treating strains of malaria that are resistant to other medications

Upstream product

• 471-46-5 Oxalamide 
• 108-88-3 toluene 
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• 10026-13-8 phosphorus pentachloride 
• 3299-61-4 N,N'-Di-p-tolyloxalamide 
• 79-37-8 oxalyl dichloride 
• 106-49-0 p-toluidine 

Downstream Products

• 157368-88-2 1,2-Bisethan-1,2-diamin 

Relevant articles and documents

Pyrrolo[3,2-b]pyrrole-based copolymers as donor materials for organic photovoltaics

A new accepter unit, pyrrolo[3,2-b]pyrrole-2,5-dione, was prepared and utilized for the synthesis of the conjugated polymers containing electron donor-acceptor pair for OPVs. Pyrrolo[3,2-b]pyrrole-2,5-dione unit, regioisomer of the known pyrrolo[3,4-c]pyrrole-1,4-dione, is originated from the structure of stable synthetic pigment. The new conjugated polymers with 1,4-diphenylpyrrolo[3,2-b]pyrrole-2,5-dione, thiophene and carbazole were synthesized using Suzuki polymerization to generate P1 and P2. The solid films of P1 and P2 show absorption bands with maximum peaks at about 377, 554 and 374, 542 nm and the absorption onsets at 670 and 674 nm, corresponding to band gaps of 1.85 and 1.84 eV, respectively. To improve the hole mobility of the polymer with 1,4-bis(4-butylphenyl)-pyrrolo[3,2-b]-pyrrole-2,5-dione unit, which was previously reported by us, the butyl group at the 4-positions of the N-substituted phenyl group was substituted with hydrogen and methyl group. The field-effect hole mobility of P2 is 9.6 × 10-5 cm2/Vs. The device with P2:PC71BM (1:2) showed VOC value of 0.84 V, JSC value of 5.10 mA/cm2, and FF of 0.33, giving PCE of 1.42%.

A new route to ring-fused pyrazines: Imidazo[4,5-b]quinoxalines by a simple oxidation-annulation sequence

Novel tricyclic 4H-imidazo[4,5-b]quinoxalines were synthesized by a new orfto-annulation process starting from 4Himidazoles and cerammonium nitrate (CAN) as oxidation reagent in the presence of potassium carbonate as base. This reaction is interpreted as

Tetrazoles: XL. Structure and basicity of 1,1′-disubstituted 5,5′-bitetrazoles

1,1′-Diaryl-5,5′-bitetrazoles, unlike 1,1′-dimethyl derivative, are Hammett bases which are much weaker than their monocyclic analogs. Bitetrazoles undergo monoprotonation in the H0 range from -5 to -9, and their pKBH+ values correla