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N-METHYL-2-MORPHOLIN-4-YLETHANAMINE is a chemical compound characterized by the molecular formula C8H17NO. It is a tertiary amine derivative that features a morpholine ring and a methyl group. N-METHYL-2-MORPHOLIN-4-YLETHANAMINE is recognized for its versatility and importance in a range of industrial applications, particularly in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

41239-40-1

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41239-40-1 Usage

Uses

Used in Pharmaceutical Industry:
N-METHYL-2-MORPHOLIN-4-YLETHANAMINE is utilized as a building block in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, enhancing their efficacy and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical sector, N-METHYL-2-MORPHOLIN-4-YLETHANAMINE serves as a key component in the creation of agrochemicals. Its role in this industry is crucial for the development of effective and environmentally friendly products for agricultural use.
Used in Organic Chemistry:
N-METHYL-2-MORPHOLIN-4-YLETHANAMINE is employed as a reagent in organic chemistry reactions. It is particularly useful in the formation of amide and ester bonds, which are fundamental in the synthesis of a wide array of organic compounds.
Used in Research and Development:
N-METHYL-2-MORPHOLIN-4-YLETHANAMINE is also valuable in research and development settings, where it can be explored for new applications and to understand its chemical properties and potential interactions with other molecules. Its use in this context aids in the advancement of scientific knowledge and the discovery of innovative applications.

Check Digit Verification of cas no

The CAS Registry Mumber 41239-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,3 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41239-40:
(7*4)+(6*1)+(5*2)+(4*3)+(3*9)+(2*4)+(1*0)=91
91 % 10 = 1
So 41239-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-8-2-3-9-4-6-10-7-5-9/h8H,2-7H2,1H3

41239-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-2-morpholin-4-ylethanamine

1.2 Other means of identification

Product number -
Other names N-Methyl-2-morpholinoethanamine

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:41239-40-1 SDS

41239-40-1Relevant academic research and scientific papers

COMPOUNDS THAT INHIBIT MCL-1 PROTEIN

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Page/Page column 743, (2018/10/25)

Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula (I), or a stereoisomer thereof; and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

Compounds and methods for inhibiting phosphate transport

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Page/Page column 234, (2016/05/02)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, wherein X, Y, A, R1 and R2 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.

SMALL MOLECULE AGONISTS OF NEUROTENSIN RECEPTOR 1

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Paragraph 00608, (2016/04/26)

Provided herein are small molecule neurotensin receptor agonists, compositions comprising the compounds, and methods of using the compounds and compositions comprising the compounds.

KINASE INHIBITORS

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Page/Page column 209; 210, (2013/06/27)

Compounds of formula (I) or a pharmaceutically acceptable salt thereof: formula (I) wherein R2, W, A, Y and R1 are as defined in the specification, are p38 MAPK inhibitors, useful as anti-inflammatory agents in the treatment of, inter alia, diseases of the respiratory tract.

KINASE INHIBITORS

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Paragraph 0830; 0831, (2013/06/27)

Compounds of formula (I) and pharmaceutically acceptable salts thereof: wherein R2, W, A, Y and R1 are as defined in the specification, are p38 MAPK inhibitors, and are useful as anti-inflammatory agents in the treatment of, inter alia, diseases of the respiratory tract.

C-4" POSITION SUBSTITUTED MACROLIDE DERIVATIVE

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Page/Page column 64, (2012/09/11)

A macrolide compound represented by the formula (I) effective against erythromycin resistant bacteria (for example, resistant pneumococci, streptococci and mycoplasmas).

COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT

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Page/Page column 72, (2012/02/01)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically ac

COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT

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Page/Page column 45-46, (2012/02/01)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically ac

COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT

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Page/Page column 52, (2012/02/01)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically ac

INHIBITORS OF ANTHRAX LETHAL FACTOR

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Page/Page column 66, (2008/06/13)

Methods, compounds and compositions for preventing and treating anthrax infections by inhibiting Anthrax Lethal Factor (LF) activity.

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