6311-48-4

Usage

Chemical Properties

Yellow solid

Upstream product

• 100-52-7 benzaldehyde 
• 64-19-7 acetic acid 
• 122-66-7 diphenyl hydrazine 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 1227476-15-4 Azobenzene 
• 64-17-5 ethanol 
• 92-87-5 p,p'-diaminobiphenyl 
• 108-94-1 cyclohexanone 
• 4335-90-4 3-benzylidene acetylacetone 

Downstream Products

• 36840-74-1 N₄,N₄'-dibenzyl-[1,1'-biphenyl]-4,4'-diamine 
• 118942-32-8 C₃₈H₂₆N₆ 
• 103777-89-5 N.N'-Bis-<α-(di-O-methyl-phosphono)-benzyl>-benzidin 

Relevant academic research and scientific papers

Asymmetric photocatalysis over robust covalent organic frameworks with tetrahydroquinoline linkage

The asymmetric photocatalytic organic synthesis (APOS) process is a sustainable and environmentally benign method for the production of optically active chemicals with sunlight as an energy source. However, it still lacks efficient semiconductors with tun

Organocatalyzed and mechanochemical solvent-free synthesis of novel and functionalized bis-biphenyl substituted thiazolidinones as potent tyrosinase inhibitors: SAR and molecular modeling studies

Eluding the involvement of solvents in organic synthesis and introducing environment friendly procedures can control environmental problems. A facile and an efficient solvent free mechanochemical method (grinding) is achieved to synthesize novel bis-biphe

Synthesis of novel bis(β-aminocarbonyl) compounds and some β-aminocarbonyls by catalyst-free multicomponent Mannich reactions

A highly diastereoselective catalyst-free multicomponent Mannich reaction between cyclohexanone, aromatic aldehydes and amines in cyclohexane is described. The double Mannich reaction of diamines and two equivalents of aldehydes and cyclohexanone gave the

Characteristic and spectroscopic properties of the Schiff-base model compounds

Two series of conjugated aromatic imines (Schiff-base model compounds) with different central groups and various side-group substitutions have been synthesized and characterized by elemental analysis, differential scanning calorimetry (DSC) technique, hyd

Organomercurials of benzidine schiff bases

Several bis-[N-benzylidene]benzidines [(p-R-C6H4CH=N-)2 benzidine, R = H(a), CH3(b), OCH3(c), NMe2(d), Cl(e) and NO2(f)] have been synthesised and reacted with Hg(OAc)2/sub

Synthesis of Novel Cyclic Formazans

The novel cyclic formazans 8,19-diaryl-6,7,9,18,20,21-hexaazapentacyclo2.52.10.132.14.17>dotriaconta-2,3,6,8,10,12,14,16,18,20,22,24,25,27,29,31-hexadecaenes (IIIa-d) and 7,21-diaryl-14-thia-6,8,9,19,20,22-hexaaz

Bis(benzylidene)benzidine Complexes of Cr(III), Mn(II), Fe(II), Fe(III), Co(II) and Ni(II)

Complexes of Cr(III), Mn(II), Fe(III), Co(II) and Ni(II) with bis(benzylidene)benzidine have been synthesized.These complexes have been assigned the formulae 2Cl2 where, M = Cr(III) and Fe(III) and 2Cl2 where, M = Mn(I

STUDIES OF SOME HETEROCYCLIC MESOGENS.

New mesogens have been prepared and studied by differential thermal analysis and optical microscopy to elucidate the effects on mesomorphic properties of replacing a benzene ring by different heterocyclic rings. To supplement earlier work and to complement the above studies of changing the terminal groups of molecules, compounds with pyridyl rings in non-terminal positions have also been studied. The overall results relating to the mesophases formed and the trends in the crystal-mesophase or -amorphous liquid and mesophase-mesophase or -amorphous liquid transition temperatures are discussed in terms of changes in axial molecular polarizability produced by the hetero-atom either directly or indirectly.