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2-(2-Methoxyphenoxy)aniline, with the molecular formula C13H13NO2, is a white to light yellow crystalline solid. It is a chemical compound that serves as an intermediate in the synthesis of dyes, pigments, and pharmaceuticals, playing a crucial role in the production of various organic compounds.

22751-09-3

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22751-09-3 Usage

Uses

Used in Chemical Synthesis:
2-(2-Methoxyphenoxy)aniline is used as a precursor in the chemical synthesis industry for the production of dyes, pigments, and pharmaceuticals. Its unique chemical structure allows it to be a key component in the creation of a wide range of organic compounds.
Used in Cosmetics Industry:
In the cosmetics industry, 2-(2-Methoxyphenoxy)aniline is used as an ingredient in hair dyes and other cosmetic products. Its ability to impart color and act as an intermediate in the formulation of these products makes it a valuable component in this sector.
Used in Pharmaceutical Industry:
2-(2-Methoxyphenoxy)aniline is also utilized in the pharmaceutical industry as an intermediate for the synthesis of various drugs. Its versatility in chemical reactions enables the development of new and effective medications.
Safety Considerations:

Check Digit Verification of cas no

The CAS Registry Mumber 22751-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,5 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22751-09:
(7*2)+(6*2)+(5*7)+(4*5)+(3*1)+(2*0)+(1*9)=93
93 % 10 = 3
So 22751-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-15-12-8-4-5-9-13(12)16-11-7-3-2-6-10(11)14/h2-9H,14H2,1H3

22751-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-METHOXYPHENOXY)ANILINE

1.2 Other means of identification

Product number -
Other names 2-amino-2'-methoxydiphenyl 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:22751-09-3 SDS

22751-09-3Downstream Products

22751-09-3Relevant articles and documents

Design, synthesis and antifungal activity of novel furancarboxamide derivatives

Wen, Fang,Jin, Hong,Tao, Ke,Hou, Taiping

, p. 244 - 251 (2016/05/24)

Twenty-seven novel furancarboxamide derivatives with a diphenyl ether moiety were synthesized and evaluated for their antifungal activity against Rhizoctonia solani, Botrytis cirerea, Valsa Mali and Sphaceloma ampelimum. Antifungal bioassay results indicated that most compounds had good or excellent fungicidal activities for R. solani and S. ampelimum at 20 mg L-1. Among synthesized compounds, compound 18e showed a greater inhibitory effect against S. ampelimum, with half maximal effective concentration (EC50) values of 0.020 mg L-1. This strong activity rivals currently used commercial fungicides, such as Boscalid and Carbendazim, and has great potential as a lead compound for future development of novel fungicides.

Four- and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches

Tietze, Lutz F.,Waldecker, Bernd,Ganapathy, Dhandapani,Eichhorst, Christoph,Lenzer, Thomas,Oum, Kawon,Reichmann, Sven O.,Stalke, Dietmar

, p. 10317 - 10323 (2015/09/01)

A highly efficient palladium-catalyzed fourfold tandem-domino reaction consisting of two carbopalladation and two C-H-activation steps was developed for the synthesis of two types of tetrasubstituted alkenes 3 and 6 with intrinsic helical chirality starting from substrates 1 and 4, respectively. A sixfold tandem-domino reaction was also developed by including a Sonogashira reaction. 20 compounds with different substitution patterns were prepared with yields of up to 97%. Structure elucidation by X-ray crystallography confirmed helical chirality of the two alkene moieties. Photophysical investigations of some of the compounds showed pronounced switching properties through light-controlled changes of their stereochemical configuration.

A Fast Way to Fluorescence: A Fourfold Domino Reaction to Condensed Polycyclic Compounds

Tietze, Lutz F.,Eichhorst, Christoph,Hungerland, Tim,Steinert, Markus

, p. 12553 - 12558 (2016/08/25)

A fast and efficient palladium-catalyzed fourfold domino Sonogashira/double-carbopalladation/C H-activation reaction that converts simple aromatic systems into complex polycyclic hydrocarbons has been developed. A number of substituted products has thus been prepared in yields up to 89 %. The structural assignment has been confirmed by using single-crystal X-ray crystallography. The products show intriguing fluorescence activity and thus might serve as chemical sensors or fluorescent imaging dyes.

Synthesis, Activity, and Molecular Modeling Studies of Novel Human Aldose Reductase Inhibitors Based on a Marine Natural Product

De La Fuente, Jesús ángel,Manzanaro, Sonia,Martín, María Jesús,De Quesada, Teresa G.,Reymundo, Isabel,Luengo, Santos M.,Gago, Federico

, p. 5208 - 5221 (2007/10/03)

Aldose reductase (ALR2) has been implicated in the etiology of diabetic complications, including blindness. Because of the limited number of currently available drugs for the prevention of these long-term complications, the discovery of new ALR2 inhibitor

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