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2-Morpholinecarboxylic acid, methyl ester (9CI) is a colorless liquid chemical compound with the molecular formula C6H11NO3. It is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a solvent and intermediate in the production of other chemical substances. Due to its potential to cause irritation to the skin, eyes, and respiratory system, and its harmful effects on aquatic organisms and the environment, it is crucial to handle 2-Morpholinecarboxylicacid,methylester(9CI) with proper safety measures and handling procedures.

135782-19-3

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135782-19-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Morpholinecarboxylic acid, methyl ester (9CI) is used as a chemical intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs and the improvement of existing ones, contributing to advancements in healthcare and medicine.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Morpholinecarboxylic acid, methyl ester (9CI) serves as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its use in this sector helps to develop more effective and safer products for agricultural applications, ensuring better crop protection and increased yields.
Used as a Solvent:
2-Morpholinecarboxylic acid, methyl ester (9CI) is utilized as a solvent in various chemical processes. Its properties make it suitable for dissolving and mixing with other substances, facilitating reactions and improving the efficiency of chemical synthesis.
Used as an Intermediate in Chemical Production:
2-Morpholinecarboxylic acid, methyl ester (9CI) is also used as an intermediate in the production of other chemical substances. Its versatility in chemical reactions allows it to be a valuable component in the synthesis of a wide range of compounds, contributing to the diversity of chemical products available in the market.

Check Digit Verification of cas no

The CAS Registry Mumber 135782-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,8 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135782-19:
(8*1)+(7*3)+(6*5)+(5*7)+(4*8)+(3*2)+(2*1)+(1*9)=143
143 % 10 = 3
So 135782-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-9-6(8)5-4-7-2-3-10-5/h5,7H,2-4H2,1H3

135782-19-3SDS

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 Methyl morpholine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Morpholinecarboxylicacid,methylester(9CI)

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:135782-19-3 SDS

135782-19-3Relevant academic research and scientific papers

JAK INHIBITOR

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Paragraph 0231; 0232; 0234, (2017/12/15)

The present invention discloses a series of JAK inhibitors, and particularly discloses a compound of formula (I) or a pharmaceutically acceptable salt thereof and the use thereof in preparation of drugs for treating diseases related to JAK.

PYRIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF PSYCHOTIC DISORDERS

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Page/Page column 42-43, (2010/11/26)

There are provided according to the invention novel compounds of formula (I) or a pharmaceutically acceptable salt thereof: (I) wherein: X represents a nitrogen atom; Y represents -C(H2)-, (-C(H2)-)2, -S(O2)- or -C(=O)-; Z represents -C(H2)-, -S(O2)-, -N(Rz)-, or an oxygen or sulphur atom; A represents hydrogen or -CH2OH; Rz represents hydrogen, C1-6 alkyl, C1-6 alkoxy, -COR7 or -SO2R7; R1 represents halogen, C1-6 alkyl, C1-6 alkoxy, =O, haloC1-6 alkyl, haloC1-6 alkoxy, hydroxyl or -CH2OH; m represents an integer from 0 to 3; R2 represents halogen, =O, C1-6alkyl (optionally substituted by one or more hydroxyl groups), -COOR7, -CONR7R8, C1-6 alkoxy, haloC1-6 alkyl, haloC1-6alkoxy or C1-6 alkyloC1-6 alkyl; n represents an integer from 0 to 3; p and q independently represent an integer from 0 to 2; R3 represents an -aryl, -heteroaryl, -heterocyclyl, -aryl-aryl, -aryl-heteroaryl, -aryl-heterocyclyl, -heteroaryl-aryl, -heteroaryl-heteroaryl, -heteroaryl-heterocyclyl, -heterocyclyl-aryl, -heterocyclyl-heteroaryl or -heterocyclyl-heterocyclyl group, all of which may be optionally substituted by one or more (e.g. 1, 2 or 3) halogen, C1-6 alkyl (optionally substituted by one or more hydroxyl groups), C3-8cycloalkyl, C1-6 alkoxy, hydroxyl, haloC1-6alkyl, haloC1-6 alkoxy, cyano, -S-C1-6 alkyl, -SO-C1-6 alkyl, -SO2-C1-6 alkyl, -COR7, -CONR7R8, -NR7R8, -NR7COC1-6 alkyl, -NR7SO2-C1-6alkyl, C1-6 alkyl-NR7R8, -OCONR7R8 , -NR7CO2R8 or -SO2NR7R8 groups; R4 and R5 independently represent C1-6 alkyl, or R4 and R5 together with the carbon atom to which they are attached may together form a C3-8cycloalkyl group; R6 represents halogen, C1-6 alkyl, C3-8cycloalkyl, C1-6 alkoxy, haloC1-6 alkyl or haloC1-6 alkoxy; s represents an integer from 0 to 4; R7 and R8 independently represent hydrogen, C1-6 alkyl or C3-8cycloalkyl; or solvates thereof.

The synthesis of 2-morpholine carboxylic acid derivatives and their elaboration to 1-aza-4-oxabicyclo[3.3.1]nonan-6-one

King,Martin

, p. 2281 - 2284 (2007/10/19)

Two syntheses of novel 2-morpholine carboxylic acid derivatives are described. The esters were converted into 1-aza-4-oxabicyclo[3.3.1]nonan-6-one, the first example of this ring system, which was further elaborated to the ortho-methoxy benzamide derivative (2).

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