122283-23-2

Basic information

• Product Name: 2-(3-METHOXYPHENOXY)BENZALDEHYDE
• Synonyms: 2-(3-Methoxyphenoxy)benzaldehyde 97%
• CAS NO: 122283-23-2
• Molecular Formula: C₁₄H₁₂O₃
• Molecular Weight: 228.24
• Product Categories: Aldehydes;C10 to C21;Carbonyl Compounds
• Mol File: 122283-23-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 34-38 °C
• Flash Point: >230 °F
• Appearance: /
• CAS DataBase Reference: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(122283-23-2)
• EPA Substance Registry System: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(122283-23-2)

Safety Data

• Hazard Codes: Xi,N
• Statements: 41-50
• Safety Statements: 26-39-60-61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 122283-23-2(Hazardous Substances Data)

Usage

Molecular Class

Benzaldehyde derivatives, which are compounds that contain a benzene ring with a formyl group (-CHO) attached to the first carbon.

Molecular Structure

A benzene ring with a methoxy group (-OCH3) attached to the third carbon and a formyl group (-CHO) attached to the first carbon.

Usage

It is commonly used in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals.

Aromatic Properties

Its aromatic structure makes it useful in the development of fragrances and flavors.

Biological and Pharmacological Activities

It has been studied for its potential biological and pharmacological activities.

Upstream product

• 150-19-6 O-methylresorcine 
• 446-52-6 2-Fluorobenzaldehyde 

Downstream Products

• 1285504-91-7 N-{(E)-3-[2-(3-methoxy-phenoxy)-phenyl]-2-methyl-acryloyl}-guanidine 
• 1285506-27-5 C₁₇H₁₆O₄ 
• 3722-52-9 3-methoxyxanthone 
• 6563-60-6 methoxy-9H-xanthen-9-one 
• 105474-96-2 2-(3-methoxyphenoxy)phenol 
• 1400883-59-1 C₂₀H₁₈O₅S 

Relevant articles and documents

Lewis Acid Catalyzed Reductive Cyclization of 2-Aryloxybenzaldehydes and 2-(Arylthio)benzaldehydes to Unsubstituted 9H-Xanthenes and Thioxanthenes in Diisopropyl Ether

Readily accessible 2-aryloxybenzaldehydes and 2-(arylthio)benzaldehydes undergo a sequence of reactions leading to a wide variety of unsubstituted 9H-xanthenes and thioxanthenes in high yields when heated with a Lewis acid in diisopropyl ether. This reductive cyclization method is compatible with several important functional groups. The method is also applicable for the selective reductive cyclization of the more electron-rich aryl ring of a 2,6-bis(aryloxy)benzaldehyde. The key feature of this transformation is the chemoselective reduction of a transient xanthylium ion in the presence of aldehydic group via intermolecular hydride transfer from diisopropyl ether (solvent). (Figure presented.).

NOVEL ACYL GUANIDINE DERIVATIVES

The present invention provides a pharmaceutical which possesses an excellent inhibitory effect on NHE3 (Na+/H+ exchanger type 3) and effectively improves diseases or conditions of organs in which NHE3 is expressed.