Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7575-35-1

Post Buying Request

7575-35-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7575-35-1 Usage

Description

2,2'-(4-Aminophenylimino)diethanol is a chemical compound with the molecular formula C10H15N2O2 and CAS number 1462-37-9. It is a diethylene glycol derivative featuring an imine group attached to a phenyl ring. 2,2'-(4-Aminophenylimino)diethanol is known for its versatile applications in various industrial and research fields.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 7575-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7575-35:
(6*7)+(5*5)+(4*7)+(3*5)+(2*3)+(1*5)=121
121 % 10 = 1
So 7575-35-1 is a valid CAS Registry Number.

7575-35-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-amino-N-(2-hydroxyethyl)anilino]ethanol

1.2 Other means of identification

Product number -
Other names 4-[di(2-hydroxyethyl)amino]-aniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7575-35-1 SDS

7575-35-1Relevant articles and documents

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

-

Paragraph 0073; 0080-0082, (2019/10/17)

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.

1,3-Dihydroxybenzene derivatives and colorants containing said compounds

-

, (2008/06/13)

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.

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

Ferlin,Via, L. Dalla,Gia

, p. 771 - 777 (2007/10/03)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7575-35-1