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4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde is a chemical compound with the molecular formula C15H19NO4. It is an aldehyde derivative of benzaldehyde, featuring a methoxy group and a morpholine group attached to the benzene ring. 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE is known for its unique chemical structure and properties, which contribute to its diverse applications across different industries.

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  • 186191-09-3 Structure
  • Basic information

    1. Product Name: 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE
    2. Synonyms: 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE;4-methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde(SALTDATA: FREE);4-methoxy-3-(2-morpholinoethoxy)benzaldehyde;IVK/4022241
    3. CAS NO:186191-09-3
    4. Molecular Formula: C14H19NO4
    5. Molecular Weight: 265.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 186191-09-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 424.5°C at 760 mmHg
    3. Flash Point: 210.5°C
    4. Appearance: /
    5. Density: 1.152g/cm3
    6. Vapor Pressure: 2.06E-07mmHg at 25°C
    7. Refractive Index: 1.543
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE(186191-09-3)
    12. EPA Substance Registry System: 4-METHOXY-3-(2-MORPHOLIN-4-YLETHOXY)BENZALDEHYDE(186191-09-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 186191-09-3(Hazardous Substances Data)

186191-09-3 Usage

Uses

Used in Organic Synthesis:
4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde is used as an intermediate in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for the creation of a wide range of compounds with specific therapeutic or functional properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde is used as a potential anticancer agent. Its biological activities have been studied, and it has shown promise in inhibiting the growth of certain cancer cells, making it a valuable compound in the development of new cancer treatments.
Used in Agrochemical Industry:
4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde is also utilized in the agrochemical industry, where it serves as a key intermediate in the synthesis of various agrochemicals. Its ability to inhibit the growth of certain pathogens makes it a valuable component in the development of pesticides and other agricultural products.
Used in Food Industry:
In the food industry, 4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde is used as a flavoring agent. Its unique chemical structure imparts specific flavor characteristics, making it a valuable ingredient in the creation of various food products.
Overall, 4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde's diverse applications in the pharmaceutical, agrochemical, and food industries are a testament to its versatility and the potential for further research and development in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 186191-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,1,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 186191-09:
(8*1)+(7*8)+(6*6)+(5*1)+(4*9)+(3*1)+(2*0)+(1*9)=153
153 % 10 = 3
So 186191-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO4/c1-17-13-3-2-12(11-16)10-14(13)19-9-6-15-4-7-18-8-5-15/h2-3,10-11H,4-9H2,1H3

186191-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxy-3-(2-morpholin-4-ylethoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:186191-09-3 SDS

186191-09-3Downstream Products

186191-09-3Relevant articles and documents

Bronchospasmolytic activity and adenosine receptor binding of some newer 1,3-dipropyl-8-phenyl substituted xanthine derivatives

Gumber, Divya,Yadav, Divya,Yadav, Rakesh,Kachler, Sonja,Klotz, Karl Norbert

, p. 600 - 609 (2020/03/23)

The aldehyde derivatives of 1,3-dipropyl xanthines as described in this paper, constitutes a new series of selective adenosine ligands displaying bronchospasmolytic activity. The effect of substitution at third- and fourth-position of 8-phenyl xanthine ha

CARBOXYLIC ACID ARYL AMIDES

-

Page/Page column 29, (2012/07/28)

Compounds of formula and pharmaceutically acceptable salts thereof are described, as well as the pharmaceutical compositions containing said compounds and their pharmaceutically acceptable salts, and the use of said compounds and pharmaceutical compositions for the treatment, control or amelioration of proliferative diseases, including cancer.

Synthesis of a series of 8-(substituted-phenyl)xanthines and a study on the effects of substitution pattern of phenyl substituents on affinity for adenosine A1 and A2A receptors

Bansal, Ranju,Kumar, Gulshan,Gandhi, Deepika,Young, Louise C.,Harvey, Alan L.

experimental part, p. 2122 - 2127 (2009/09/30)

A new series of 8-(substituted-phenyl)xanthines have been synthesized and compounds were evaluated for their affinity for A1 and A2 adenosine receptors (AR) using radioligand binding assays. The effects of varying the positions of 8-phenyl substituents on affinity and selectivity at A1 and A2A adenosine receptors have been studied. Isovanilloid 1,3-dimethyl-8-[4-methoxy-3-(2-morpholin-4-ylethoxy)phenylxanthine (9d) displayed the highest affinity and selectivity towards A2A AR subtypes with Ki = 100 nM over A1 receptors (Ki > 100 mM). It has been observed that substitution pattern on 8-phenyl group greatly affects the affinity and selectivity at adenosine receptors, with A2A tolerating bulkier substituents than did A1 receptors.

Small molecule thienopyrimidine-based protein tyrosine kinase inhibitors

-

Page/Page column 41, (2010/02/15)

Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.

6-aryl pyrazolo?3,4-D! pyrimidin-4-ones and compositions and method of use thereof

-

, (2008/06/13)

6-Aryl pyrazolo?3,4-d!pyrimidin-4-one derivatives, pharmaceutical compositions containing them and methods for effecting c-GMP-phosphodiesterase inhibition and for treating heart failure and/or hypertension.

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