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4-(2-aminopropyl)morpholine, also known as 2-(3-morpholinopropyl)amine, is a chemical compound with the formula C7H16N2O. It is a morpholine derivative featuring an amine functional group attached to a propyl chain, known for its stabilizing and chelating properties, which makes it valuable in various chemical processes and formulations.

50998-05-5

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50998-05-5 Usage

Uses

Used in Pharmaceutical Synthesis:
4-(2-aminopropyl)morpholine is used as an intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex organic compounds, contributing to the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 4-(2-aminopropyl)morpholine serves as an intermediate, aiding in the production of various agrochemicals that are essential for crop protection and enhancement of agricultural yields.
Used as a Corrosion Inhibitor in Industrial Applications:
4-(2-aminopropyl)morpholine is utilized as a corrosion inhibitor, protecting materials from degradation in industrial settings, thereby extending the lifespan of equipment and structures.
Used in Chemical Processes and Formulations:
Due to its stabilizing and chelating properties, 4-(2-aminopropyl)morpholine is employed in various chemical processes to ensure the stability and effectiveness of formulations, enhancing the performance of end products.
It is crucial to handle 4-(2-aminopropyl)morpholine with care, considering its potential hazards and adverse effects if not used properly, ensuring safety in all applications.

Check Digit Verification of cas no

The CAS Registry Mumber 50998-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50998-05:
(7*5)+(6*0)+(5*9)+(4*9)+(3*8)+(2*0)+(1*5)=145
145 % 10 = 5
So 50998-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-7(8)6-9-2-4-10-5-3-9/h7H,2-6,8H2,1H3

50998-05-5 Well-known Company Product Price

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  • Aldrich

  • (CBR00001)  1-(4-Morpholinyl)-2-propanamine  AldrichCPR

  • 50998-05-5

  • CBR00001-1G

  • 4,512.69CNY

  • Detail

50998-05-5SDS

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 1-(4-Morpholinyl)-2-propanamine

1.2 Other means of identification

Product number -
Other names 1-morpholin-4-ylpropan-2-amine

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:50998-05-5 SDS

50998-05-5Relevant academic research and scientific papers

THIADIAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

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Page/Page column 19, (2010/06/22)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted thiadiazolyl, and R2, R3, R4, R5, R6, R7 and R8 are as defined herein. Also disclosed are methods of using the compounds for treating diseases associated with P2X3 and/or a P2X2/3 receptor antagonists and methods of making the compounds.

PYRIMIDINES WITH TIE2 (TEK) ACTIVITY

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Page/Page column 135, (2010/02/12)

The invention relates to a compound of the Formula (I). or salt thereof wherein R1, R2, R3, R4, R5, R6, A, B, L, n and m are as defined in the description. The invention also relates to pharmaceutical compositions of said compounds, the use of said compounds as medicaments and in the production of an anti-angiogenic effect in a warm-blooded animal. The invention also relates to processes for the preparation of said compounds.

Nosylaziridines: Activated aziridine electrophiles

Maligres, Peter E.,See, Marjorie M.,Askin, David,Reider, Paul J.

, p. 5253 - 5256 (2007/10/03)

Nosylaziridines are highly reactive electrophiles towards a variety of nucleophiles yielding the corresponding SN2 adducts without competing attack on the nosyl functionality (SNAr). The resulting primary nosylamide adducts can he readily cleaved under mild conditions to provide the primary amines.

DIRECT NUCLEOPHILIC SUBSTITUTION IN 2-HALOALKYLAMINES: NEW ROUTE TO SUBSTITUTED ETHYLENEDIAMINES

Chechik, V. O.,Bobylev, V. A.

, p. 1501 - 1502 (2007/10/03)

Nucleophilic substitution in 2-haloalkylamines in weakly polar media was found to proceed partially without intermediate formation of aziridines.This makes it possible to obtain pure substituted ethylenediamines.

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