Welcome to LookChem.com Sign In|Join Free
  • or
Methyl 3-(morpholin-4-yl)prop-2-enoate is a chemical compound with the molecular formula C9H15NO3. It is an acrylate ester characterized by the presence of a methyl group, a morpholine ring, and an acrylate group. This versatile compound is widely used in the synthesis of pharmaceuticals, agrochemicals, and materials, serving as a valuable building block in organic synthesis. Its applications extend to the production of polymers, advanced materials, catalysts, and as an intermediate in the synthesis of bioactive compounds, making it an essential component in the chemical industry.

1009-80-9

Post Buying Request

1009-80-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1009-80-9 Usage

Uses

Used in Pharmaceutical Synthesis:
Methyl 3-(morpholin-4-yl)prop-2-enoate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to enhance the properties of drug molecules and facilitate the development of new therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, methyl 3-(morpholin-4-yl)prop-2-enoate is utilized as a building block in the creation of effective and environmentally friendly pesticides and other agrochemical products, contributing to sustainable agricultural practices.
Used in Material Science:
Methyl 3-(morpholin-4-yl)prop-2-enoate is employed as a component in the production of polymers and advanced materials, such as coatings, adhesives, and composites, due to its ability to improve material properties and performance.
Used in Catalyst Development:
methyl 3-(morpholin-4-yl)prop-2-enoate is used as a precursor in the development of highly efficient catalysts, which are essential in various chemical reactions and processes, enhancing the overall efficiency and selectivity of these reactions.
Used in Organic Synthesis:
Methyl 3-(morpholin-4-yl)prop-2-enoate serves as a versatile building block in organic synthesis, allowing for the creation of a wide range of chemical compounds and products across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1009-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1009-80:
(6*1)+(5*0)+(4*0)+(3*9)+(2*8)+(1*0)=49
49 % 10 = 9
So 1009-80-9 is a valid CAS Registry Number.

1009-80-9SDS

SAFETY DATA SHEETS

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.Identification

1.1 GHS Product identifier

Product name methyl 3-morpholin-4-ylprop-2-enoate

1.2 Other means of identification

Product number -
Other names Methyl4-morpholineacrylate

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:1009-80-9 SDS

1009-80-9Relevant academic research and scientific papers

Diastereoselective synthesis of functionalized tetrahydropyrimidin-2- thiones via ZnCl2 promoted one-pot reactions

Liu, Zhenming,Zhang, Lili,Sun, Jing,Yan, Chaoguo

, p. 172 - 178 (2014)

In the presence of zinc chloride, the in situ generated β-enamino ester from the reaction of morpholine, piperidine and pyrrolidine with methyl propiolate reacted, with aromatic aldehydes and thiourea in ethanol resulting in the functionalized tetrahydrop

NNN-pincer-copper complex immobilized on magnetic nanoparticles as a powerful hybrid catalyst for aerobic oxidative coupling and cycloaddition reactions in water

Zohreh, Nasrin,Jahani, Mahboobeh

, p. 117 - 129 (2017)

A simple and reliable methodology is described for preparing the first heterogeneous NNN-pincer-copper hybrid catalyst with a high control over surface composition. The strategy relies on the covalently bonding of 2-aminopyridine to cyanuric chloride-functionalized magnetic nanoparticles followed by complexation with CuI. These claims are confirmed by different characterization methods such as SEM, TEM, FT-IR, TGA, ICP, XRD, and elemental analysis. The finely engineered supported catalyst is employed in the aerobic oxidative coupling of terminal alkynes and click reaction using only 0.38 and 0.04 mol% catalyst, respectively. All reactions perform under solvent-free condition or green solvent H2O. Also, the catalyst is readily recovered and reused for up to 8 and 6 subsequent runs in click and homocoupling reactions without significant loss of activity or leaching.

CINNOLINES AS INHIBITORS OF HPK 1

-

Page/Page column 49-50, (2021/01/29)

Compounds of Formula (I) or (Ia), pharmaceutically acceptable salts, stereoisomers, tautomers, solvates or prodrugs, and their use as HPK1 inhibitors are described herein, and also described are methods for preparing the compounds, and methods of treating HPK1-dependent diseases or disorders, such as cancer.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1009-80-9