Welcome to LookChem.com Sign In|Join Free

CAS

  • or

122283-23-2

2-(3-METHOXYPHENOXY)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122283-23-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 122283-23-2 Structure

  • Basic information

    1. Product Name: 2-(3-METHOXYPHENOXY)BENZALDEHYDE
    2. Synonyms: 2-(3-Methoxyphenoxy)benzaldehyde 97%
    3. CAS NO:122283-23-2
    4. Molecular Formula: C14H12O3
    5. Molecular Weight: 228.24
    6. EINECS: N/A
    7. Product Categories: Aldehydes;C10 to C21;Carbonyl Compounds
    8. Mol File: 122283-23-2.mol

  • Chemical Properties

    1. Melting Point: 34-38 °C
    2. Boiling Point: N/A
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(122283-23-2)
    11. EPA Substance Registry System: 2-(3-METHOXYPHENOXY)BENZALDEHYDE(122283-23-2)

  • Safety Data

    1. Hazard Codes: Xi,N
    2. Statements: 41-50
    3. Safety Statements: 26-39-60-61
    4. RIDADR: UN 3077 9/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 122283-23-2(Hazardous Substances Data)

122283-23-2 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.

Check Digit Verification of cas no

The CAS Registry Mumber 122283-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122283-23:
(8*1)+(7*2)+(6*2)+(5*2)+(4*8)+(3*3)+(2*2)+(1*3)=92
92 % 10 = 2
So 122283-23-2 is a valid CAS Registry Number.

122283-23-2SDS

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-(3-METHOXYPHENOXY)BENZALDEHYDE

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-(3-methoxyphenoxy)

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:122283-23-2 SDS

122283-23-2Relevant articles and documents

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

Verma, Shashi Kant,Prajapati, Anamika,Saini, Manoj Kumar,Basak, Ashok K.

supporting information, p. 532 - 539 (2020/11/30)

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.).

Metal-free oxidative coupling: Xanthone formation via direct annulation of 2-aryloxybenzaldehyde using tetrabutylammonium bromide as a promoter in aqueous medium

Rao, Honghua,Ma, Xinyi,Liu, Qianzi,Li, Zhongfeng,Cao, Shengli,Li, Chao-Jun

supporting information, p. 2191 - 2196 (2013/10/01)

A metal-free intramolecular annulation of 2-aryloxybenzaldehydes to xanthones is disclosed, which proceeds through the direct oxidative coupling of an aldehyde C-H bond and aromatic C-H bonds using tetrabutylammonium bromide (TBAB) as a promoter in aqueous medium. This strategy works smoothly in the presence of both electron-donating and electron-withdrawing groups, and displays good tolerance towards catalytically reactive substituents, thus promising further functionalizations of xanthone products.

NOVEL ACYL GUANIDINE DERIVATIVES

-

Page/Page column 26, (2011/04/24)

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.

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 122283-23-2