4182-45-0

Usage

Physical state

Colorless to light yellow liquid

Odor

Strong

Uses

a. Building block in pharmaceuticals production
b. Building block in agrochemicals production
c. Building block in dyes production
d. Curing agent for epoxy resins
e. Corrosion inhibitor

Hazardous properties

Can cause skin and eye irritation, respiratory and allergic reactions in humans

Safety precautions

Should be handled with care, used in a properly equipped laboratory, and only by trained individuals.

Upstream product

• 20727-35-9 N,N'-(3-phenyl-3-aza-pentane-1,5-diyl)-bis-phthalimide 
• 10035-10-6 hydrogen bromide 
• 3590-12-3 N,N-bis(2-p-tolylsulfonyloxyethyl)aniline 
• 61793-99-5 3,3'-phenylimino-di-propionic acid diethyl ester 
• 56329-74-9 3,3′-(phenylazanediyl)dipropanehydrazide 
• 62-53-3 aniline 
• 99169-09-2 N,N-bis(2-azidoethyl)aniline 

Downstream Products

• 63632-77-9 2-Ethyl-N-(2-{[2-(2-ethyl-butyrylamino)-ethyl]-phenyl-amino}-ethyl)-butyramide 
• 63632-95-1 (E)-Undec-2-enoic acid (2-{phenyl-[2-((E)-undec-2-enoylamino)-ethyl]-amino}-ethyl)-amide 
• 46992-64-7 Phenyl-bis-(2-guanidino-ethyl)-amin 
• 132066-06-9 N,N'-[(phenylimino)diethane-2,1-diyl]bis(4-methylbenzenesulfonamide) 
• 1664-40-0 N-(2-aminoethyl)benzeneamine 
• 874280-56-5 C₄₀H₇₁N₅O₄ 
• 874280-57-6 C₂₀H₃₁N₅O₄ 
• 1491140-89-6 C₃₄H₃₇N₇ 
• 1450913-20-8 C₃₅H₃₇N₇O 
• 1450913-22-0 C₄₂H₄₅N₈⁽¹⁺⁾ 
• 1450913-23-1 C₄₂H₄₅N₈⁽¹⁺⁾ 
• 1450913-32-2 C₄₆H₄₇N₈⁽¹⁺⁾ 
• 1450913-33-3 C₄₆H₄₇N₈⁽¹⁺⁾ 
• 1450913-34-4 C₄₇H₄₉N₈O⁽¹⁺⁾ 

Relevant academic research and scientific papers

Focused fluorescent probe library for metal cations and biological anions

A focused fluorescent probe library for metal cations was developed by combining metal chelators and picolinium/quinolinium moieties as combinatorial blocks connected through a styryl group. Furthermore, metal complexes derived from metal chelators having high binding affinities for metal cations were used to construct a focused probe library for phosphorylated biomolecules. More than 250 fluorescent probes were screened for identifying an ultraselective probe for dTTP.

Synthesis and characterization of N-substitutional ethylenediamine derivatives

N-Substituted and N,N-disubstituted ethylenediamine derivatives were prepared rapidly in aqueous conditions from 30 to 76 % yields, respectively, on a multi-gram scale starting from inexpensive and commercially available starting materials. The steps involved Michael addition, hydrazinolysis and Curtius rearrangements. The highlight of this method lies on its convenience and economy in accessing these intermediates.

Azobenzene coupled chromogenic receptors for the selective detection of copper(II) and its application as a chemosensor kit

Azobenzene-based receptors 1-4 as colorimetric sensing materials were synthesized and their sensing properties were examined. In solution, the proposed sensing materials give rise to a large cation-induced hypochromic shift for Cu2+ resulting i