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102-56-7 Usage


2,5-Dimethoxyaniline is an organic compound characterized by its grey to dark brown crystalline powder or lumps. It is known for its unique chemical properties and potential applications in various industries.


Used in Enzyme Induction:
2,5-Dimethoxyaniline is used as a laccase inducer for immobilizing the enzyme laccase from Trumetes versicolor. This application is particularly relevant in the field of biotechnology and enzyme research, where the compound plays a crucial role in enhancing the efficiency and stability of the enzyme.
Used in Chemical Synthesis:
As an organic compound, 2,5-Dimethoxyaniline can be utilized in the synthesis of various chemical products, such as dyes, pigments, and pharmaceuticals. Its unique chemical properties make it a valuable intermediate in the production of these substances.
Used in Analytical Chemistry:
The compound's distinct characteristics also make it suitable for use in analytical chemistry, where it can be employed as a reagent or a reference material in various analytical techniques.
Used in Research and Development:
Due to its unique properties, 2,5-Dimethoxyaniline can be a valuable asset in research and development, particularly in the fields of material science, pharmaceuticals, and environmental science. It can be used to study the interactions between different molecules and to develop new methods for synthesizing and characterizing novel compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 102-56-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102-56:
27 % 10 = 7
So 102-56-7 is a valid CAS Registry Number.

102-56-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L05053)  2,5-Dimethoxyaniline, 99%   

  • 102-56-7

  • 50g

  • 284.0CNY

  • Detail
  • Alfa Aesar

  • (L05053)  2,5-Dimethoxyaniline, 99%   

  • 102-56-7

  • 250g

  • 647.0CNY

  • Detail



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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017


1.1 GHS Product identifier

Product name 2,5-Dimethoxyaniline

1.2 Other means of identification

Product number -
Other names Aminohydroquinone dimethyl ether

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:102-56-7 SDS

102-56-7Relevant articles and documents

Methoxy and bromo scans on N-(5-methoxyphenyl) methoxybenzenesulphonamides reveal potent cytotoxic compounds, especially against the human breast adenocarcinoma MCF7 cell line

González, Myriam,Ovejero-Sánchez, María,Vicente-Blázquez, Alba,Medarde, Manuel,González-Sarmiento, Rogelio,Peláez, Rafael

, p. 1029 - 1047 (2021/06/16)

Thirty seven N-(5-methoxyphenyl)-4-methoxybenzenesulphonamide with methoxy or/and bromo substitutions (series 1-4) and with different substituents on the sulphonamide nitrogen have been synthesised. 21 showed sub-micromolar cytotoxicity against HeLa and HT-29 human tumour cell lines, and were particularly effective against MCF7. The most potent series has 2,5-dimethoxyanilines, especially the 4-brominated compounds 23–25. The active compounds inhibit microtubular protein polymerisation at micromolar concentrations, thus pointing at tubulin as the target. Co-treatment with the MDR inhibitor verapamil suggests that they are not MDR substrates. Compound 25 showed nanomolar antiproliferative potency. It severely disrupts the microtubule network in cells and arrests cells at the G2/M cell-cycle phase, thus confirming tubulin targeting. 25 triggered apoptotic cell death, and induced autophagy. Docking studies suggest binding in a distinct way to the colchicine site. These compounds are promising new antitumor agents acting on tubulin.



Paragraph 0098; 0134; 0135; 0165, (2018/03/25)

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds

Gao, Hongyin,Zhou, Zhe,Kwon, Doo-Hyun,Coombs, James,Jones, Steven,Behnke, Nicole Erin,Ess, Daniel H.,Kürti, László

, p. 681 - 688 (2017/06/30)

Arylmetals are highly valuable carbon nucleophiles that are readily and inexpensively prepared from aryl halides or arenes and widely used on both laboratory and industrial scales to react directly with a wide range of electrophiles. Although C-C bond formation has been a staple of organic synthesis, the direct transfer of primary amino (-NH2) and hydroxyl (-OH) groups to arylmetals in a scalable and environmentally friendly fashion remains a formidable synthetic challenge because of the absence of suitable heteroatom-transfer reagents. Here, we demonstrate the use of bench-stable N-H and N-alkyl oxaziridines derived from readily available terpenoid scaffolds as efficient multifunctional reagents for the direct primary amination and hydroxylation of structurally diverse aryl- and heteroarylmetals. This practical and scalable method provides one-step synthetic access to primary anilines and phenols at low temperature and avoids the use of transition-metal catalysts, ligands and additives, nitrogen-protecting groups, excess reagents and harsh workup conditions.

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