7575-35-1

Usage

Uses

Used in Metal Ion Extraction and Purification:
2,2'-(4-Aminophenylimino)diethanol is used as a chelating agent for metal ion extraction and purification processes. Its ability to form stable complexes with metal ions makes it a valuable tool in this application.
Used in Coordination Compounds:
2,2'-(4-Aminophenylimino)diethanol serves as a ligand for coordination compounds, playing a crucial role in the formation and stabilization of these compounds.
Used in Organic Synthesis:
2,2'-(4-Aminophenylimino)diethanol is utilized as a building block in the synthesis of various organic compounds, contributing to the development of new chemical entities.
Used in Specialty Chemicals and Pharmaceuticals Production:
2,2'-(4-Aminophenylimino)diethanol is employed in the production of specialty chemicals and pharmaceuticals, where its unique properties and reactivity are harnessed to create novel products.

Upstream product

• 18226-17-0 N,N-bis(2-hydroxyethyl)-4-nitroaniline 
• 350-46-9 4-Fluoronitrobenzene 
• 100-00-5 4-chlorobenzonitrile 
• 120-07-0 2,2'-(phenylimino)bis[ethanol] 

Downstream Products

• 55302-73-3 C₁₈H₂₂N₂O₃ 
• 55302-65-3 C₁₇H₂₀N₄O₄ 
• 55302-71-1 C₁₈H₂₂N₄O₄ 
• 55302-66-4 C₂₀H₂₅N₃O₄ 
• 125174-08-5 N,N-bis(2-hydroxyethyl)-4-<5-pentanamido>aniline 
• 135508-72-4 (6R,7R)-3-{4-[Bis-(2-hydroxy-ethyl)-amino]-phenylcarbamoyloxymethyl}-8-oxo-7-(2-thiophen-2-yl-acetylamino)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 
• 3009-34-5 quinoneimine 
• 24093-23-0 N¹--2-amino-p-benzochinon-diimin 
• 102974-74-3 2-[{4-[2-Amino-4-imino-cyclohexa-2,5-dien-(Z)-ylideneamino]-phenyl}-(2-hydroxy-ethyl)-amino]-ethanol 
• 102139-55-9 4'-bis-(2-hydroxyethylamino)-2,4-dinitrodiphenylamine 
• 524734-89-2 1-methyl-4-nitro-1H-pyrrole-2-carboxylic acid {4-[bis-(2-hydroxy-ethyl)-amino]-phenyl}-amide 
• 244247-69-6 4-bis(2'-hydroxyethyl)amino-N-tert-butyloxycarbonylaniline 
• 304015-75-6 (5-nitro-2-furyl)methyl 4-[bis(2-hydroxyethyl)amino]phenylcarbamate 
• 304015-77-8 (5-nitro-2-thienyl)methyl 4-[bis(2-hydroxyethyl)amino]phenylcarbamate 

Relevant academic research and scientific papers

Hydrogen peroxide-responsive nitrogen mustard anti-tumor pro-drug and preparation method thereof

The invention discloses a hydrogen peroxide-responsive nitrogen mustard anti-tumor pro-drug and a preparation method thereof, and belongs to the field of pharmaceutical chemistry. The compound contains an alpha-ketoamide structure and a nitrogen mustard structure, can rapidly respond to H2O2, can be used as the nitrogen mustard anti-tumor pro-drug, has good response effect to H2O2, has high cell selectivity and small toxic and side effects, provides an effective, safe and highly selective anti-tumor drug, enriches the types of nitrogen mustard anti-tumor drugs, and has a good market prospect.

2, 4 -DIAMINOPYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

The present invention relates to novel pyrimide derivatives of formula (I): that are useful as kinase inhibitors. More particularly, the present invention relates to novel pyrimidine compounds, methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of proliferative disorders.

Synthesis and antiproliferative activity of some new DNA-targeted alkylating pyrroloquinolines

Two novel DNA-direct alkylating agents, consisting of aniline mustard linked to an angular 3H-pyrrolo[3,2-f]quinoline nucleus, were synthetized and assayed for their in vitro antiproliferative activity. Simple convergent synthesis, consisting of separate preparation of 9-chloro-3H-pyrrolo[3,2-f] quinoline and p-amino-aniline derivatives, and following their linkage by substitution reactions 8a, b and 10, yielded the corresponding diol derivatives 7b and 9. Biological properties were evaluated with respect to cell growth inhibition, ability to form cross-links with DNA, and capacity to give rise to a molecular complex with the macromolecule for 7b, 8b, 9 and 10.

1,3-Dihydroxybenzene derivatives and colorants containing said compounds

1,3-Dihydroxybenzene derivatives of general formula (I) or (Ia) or physiologically tolerated, water-soluble thereof wherein R′1 denotes substituted pyridyl group, a pyrimidyl group, a group of formula (IIa) or (IIIa) and the dyeing agents for keratin fibers containing these compounds.

One step hair coloring compositions using salts

A hair coloring composition comprising the following two compositions which are mixed just prior to application to the hair: (a) a composition comprising a water-soluble peroxygen oxidizing agent; and (b) a composition comprising one or more oxidative hair coloring agents selected from the group consisting of an aromatic diamine, an amino phenol, a naphthol, a polyhydric phenol, a catechol and mixtures thereof; wherein the composition comprising one or more oxidative hair coloring agents further comprises al least one water soluble carbonate releasing salts; and optionally a water soluble ammonium salt, is described.

Transition metal complexes as dye forming catalysts in hair coloring compositions

A hair coloring composition comprising a first composition which comprises: (a) a dye forming transition metal salt or complex; which is first applied to the hair; and a second composition which comprises the following two compositions which are mixed just prior to application to the hair: (a) a composition comprising a water-soluble peroxygen oxidizing agent; and (b) a composition comprising one or more oxidative hair coloring agents selected from the group consisting of an aromatic diamine, an aminophenol, a polyhydric phenol a catechol and mixtures thereof.

Enhanced color deposition for hair with sequestering agents

Hair coloring compositions which comprise: (A) non-nitrogenous chelating agents from the group consisting of polyphosphate; phosphonates; hydroxycarboxylates; polyacrylates; zeolite; and mixtures thereof; (B) an oxidative dye primary intermediate; and (C) an oxidative dye coupler; (D) and water are described. The present invention also relates to a method for coloring hair which comprises contacting said hair with a hair coloring composition as described above.

Means and method for dying keratinic fibers

Composition for coloring keratin fibers based on a developer-coupler combination characterized in that it contains as the coupler 3-(2,4-diaminophenoxy)-1-propanol and as the developer a p-phenylenediamine derivative monosubstituted on the benzene ring and having general formula (I) ?and/or a 4,5-diamino-1H-pyrazole derivative of general formula (II) ?and/or a p-aminophenol derivative of general formula (III) ?as well as a method for the oxidative coloring of hair, and the use of said composition.

1,4-diazacycloheptane derivatives and their use in hair oxidation dyes

A 1,4-diazacycloheptane derivative and an oxidative hair colorant containing the derivative as a primary intermediate is presented. The 1,4-diazacycloheptane derivative is of the formula: STR1 where R1, R2, R3 and R4 independently of one another represent hydrogen, a C1-4 alkyl or hydroxyalkyl group or a C2-4, dihydroxyalkyl group, X and Y independently of one another represent hydrogen, chlorine, fluorine, a C1-4 alkyl, hydroxyalkyl, aminoakyl or alkoxy group, a C2-4 dihydroxyalkyl group or an allyl group and R5 and R6 independently of one another represent hydrogen or a C1-4 alkyl group. Natural color tones can be obtained in keratin fibers with oxidative hair colorants containing the 1,4-diazacycloheptane derivative, without the use of additional primary intermediates.

Process for dyeing keratinous fibers with aminoindoles and oxidation dye precursors at basic Ph's and dyeing agents

The invention relates to a process for dyeing keratinous fibres, which consists in applying to these fibres a composition containing, in a suitable medium for dyeing, at least one coupler of formula: STR1 where R1 denotes hydrogen or alkyl, R2 and R3 denote hydrogen, alkyl, COOR' where R' is alkyl or hydrogen, at least one of the groups R2 and R3 denoting hydrogen, R4 denotes hydrogen, alkyl, hydroxyalkyl, polyhydroxyalkyl or aminoalkyl, Z1 and Z2 denote hydrogen, alkyl, hydroxyl, halogen, alkoxy, at least one of the groups Z1 and Z2 is other than hydrogen at least one oxidation dye precursor, at least one oxidizing agent, the pH of the composition applied to the fibres being higher than 7.