Welcome to LookChem.com Sign In|Join Free
  • or
[4-(2-MORPHOLINOETHOXY)PHENYL]METHYLAMINE is a chemical compound characterized by a phenyl ring connected to a methylamine group via a morpholinoethoxy bridge. This unique structure endows it with potential pharmacological properties, making it a promising candidate in medicinal chemistry and drug development. The presence of the morpholino group indicates possible biological activity, suggesting its utility as a building block for synthesizing innovative pharmaceutical compounds. Further exploration of this molecule could pave the way for the creation of new therapeutic agents to address a range of diseases and conditions.

140836-69-7

Post Buying Request

140836-69-7 Suppliers

Recommended suppliers

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

140836-69-7 Usage

Uses

Used in Medicinal Chemistry:
[4-(2-MORPHOLINOETHOXY)PHENYL]METHYLAMINE is used as a chemical intermediate for the synthesis of novel pharmaceutical compounds due to its unique structure and potential biological activity.
Used in Drug Development:
In the pharmaceutical industry, [4-(2-MORPHOLINOETHOXY)PHENYL]METHYLAMINE is utilized as a precursor in the development of new therapeutic agents, leveraging its potential pharmacological properties to target various diseases and conditions.
Used in Research and Development:
[4-(2-MORPHOLINOETHOXY)PHENYL]METHYLAMINE serves as a subject of research for understanding its biological activity and exploring its potential applications in creating new treatments, thus contributing to the advancement of medical science.

Check Digit Verification of cas no

The CAS Registry Mumber 140836-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,3 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140836-69:
(8*1)+(7*4)+(6*0)+(5*8)+(4*3)+(3*6)+(2*6)+(1*9)=127
127 % 10 = 7
So 140836-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2O2/c14-11-12-1-3-13(4-2-12)17-10-7-15-5-8-16-9-6-15/h1-4H,5-11,14H2

140836-69-7SDS

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 [4-(2-morpholin-4-ylethoxy)phenyl]methanamine

1.2 Other means of identification

Product number -
Other names Benzenemethanamine,4-[2-(4-morpholinyl)ethoxy]

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:140836-69-7 SDS

140836-69-7Relevant academic research and scientific papers

Solid dispersions containing an apoptosis-inducing agent

-

Page/Page column 137; 138, (2019/03/15)

A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer.

Cobalt-based nanoparticles prepared from MOF-carbon templates as efficient hydrogenation catalysts

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Sohail, Manzar,Alshammari, Ahmad S.,Pohl, Marga-Martina,Beller, Matthias,Jagadeesh, Rajenahally V.

, p. 8553 - 8560 (2018/11/30)

The development of efficient and selective nanostructured catalysts for industrially relevant hydrogenation reactions continues to be an actual goal of chemical research. In particular, the hydrogenation of nitriles and nitroarenes is of importance for the production of primary amines, which constitute essential feedstocks and key intermediates for advanced chemicals, life science molecules and materials. Herein, we report the preparation of graphene shell encapsulated Co3O4- and Co-nanoparticles supported on carbon by the template synthesis of cobalt-terephthalic acid MOF on carbon and subsequent pyrolysis. The resulting nanoparticles create stable and reusable catalysts for selective hydrogenation of functionalized and structurally diverse aromatic, heterocyclic and aliphatic nitriles, and as well as nitro compounds to primary amines (>65 examples). The synthetic and practical utility of this novel non-noble metal-based hydrogenation protocol is demonstrated by upscaling several reactions to multigram-scale and recycling of the catalyst.

Method for inhibiting neoplastic cells and related conditions by exposure to substituted N- arylmethyl and heterocyclmethyl-1H-pyrazolo (3,4-B) quinolin-4-amines

-

, (2008/06/13)

A method for inhibiting neoplastic cells and related conditions by exposing them to substituted N-arylmethyl and heterocyclmethyl-1H-pyrazolo?3,4-B!quinolin-4-amines.

Substituted N-arylmethyl and heterocyclmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines and compositions and methods of use thereof

-

, (2008/06/13)

Substituted N-arylmethyl and heterocyclylmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines, pharmaceutical compositions containing them and methods for a) effecting c-GMP-phosphodiesterase inhibition, b) treating heart failure and/or hypertension, c) reversing o

Synthesis, gastrointestinal prokinetic activity and structure-activity relationships of novel N-[[2-(dialkylamino)ethoxy]benzyl]benzamide derivatives

Sakaguchi,Nishino,Ogawa,Iwanaga,Yasuda,Kato,Ito

, p. 202 - 211 (2007/10/02)

Novel N-[[2-(dialkylamino)ethoxy]benzyl]benzamide derivatives (II-1-51), derived from the structural modification of metoclopramide (1), were synthesized and examined for their pharmacological activities. Among them, N-[4-[2-(dimethylamino)ethoxy]benzyl]-3,4-dimethoxybenzamide (II-34) which exhibited well balanced gastrointestinal prokinetic and antiemetic activities was selected as a new type of gastrointestinal prokinetic agent.

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 140836-69-7