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4-[[4-(morpholin-4-ylmethyl)phenyl]methyl]morpholine is a complex organic compound with the molecular formula C18H26N2O2. It is a derivative of morpholine, a heterocyclic compound with a five-membered ring containing two nitrogen atoms. The structure of 4-[[4-(morpholin-4-ylmethyl)phenyl]methyl]morpholine features a morpholine ring attached to a benzene ring through a methylene bridge, with another morpholine ring connected to the benzene ring through a second methylene bridge. 4-[[4-(morpholin-4-ylmethyl)phenyl]methyl]morpholine is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal compounds. Its unique structure allows for the formation of multiple hydrogen bonds, which can be beneficial in the design of molecules that interact with biological targets.

6425-53-2

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6425-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6425-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6425-53:
(6*6)+(5*4)+(4*2)+(3*5)+(2*5)+(1*3)=92
92 % 10 = 2
So 6425-53-2 is a valid CAS Registry Number.

6425-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(morpholin-4-ylmethyl)phenyl]methyl]morpholine

1.2 Other means of identification

Product number -
Other names 4,4'-[1,4-phenylenebis(methylene)]dimorpholine

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:6425-53-2 SDS

6425-53-2Downstream Products

6425-53-2Relevant academic research and scientific papers

BIS-AMINES, COMPOSITIONS, AND USES RELATED TO CXCR4 INHIBITION

-

Page/Page column 65, (2017/02/09)

This disclosure relates bis-amine compounds disclosed herein and uses related to CXCR4 inhibition. In certain embodiments, the compounds have formula (I), salts, derivatives, and prodrugs thereof wherein, A is a bridging aryl or heterocyclyl and R1 and R2 are further disclosed herein. In certain embodiments, the disclosure contemplates pharmaceutical compositions comprising compounds disclosed herein. In certain embodiments, the disclosure relates to methods of treating or preventing CXCR4 related diseases or conditions by administering an effective amount of a compound disclosed herein to a subject in need thereof.

Symmetrical bis-tertiary amines as novel CXCR4 inhibitors

Bai, Renren,Liang, Zhongxing,Yoon, Younghyoun,Liu, Shuangping,Gaines, Theresa,Oum, Yoonhyeun,Shi, Qi,Mooring, Suazette Reid,Shim, Hyunsuk

, p. 340 - 350 (2016/05/24)

CXCR4 inhibitors are promising agents for the treatment of cancer metastasis and inflammation. A series of novel tertiary amine derivatives targeting CXCR4 were designed, synthesized, and evaluated. The central benzene ring linker and side chains were mod

Synthesis of novel aromatic core zero generation dendrimers

Füst?s, Melinda-Emese,Sipos, Tmea-Anita,Diudea, Mircea V.,Katona, Gabriel

, p. 129 - 132 (2015/08/06)

Bromomethyl arenes used as polyfunctional core of dendrimers were derivatized with diethanolamine branches. The obtained compounds containing 4 or 6 hydroxyl terminal surface groups are highly water-soluble.

A fast and highly efficient method for the synthesis of tertiary amines in aqueous medium

Adimurthy, Subbarayappa,Joshi, Girdhar

experimental part, p. 771 - 775 (2011/01/04)

A facile and highly efficient method for the synthesis of tertiary amines by the reaction of secondary amines with benzylic bromides and 1,1'-dibromo p/o-xylenes in aqueous dioxane and NaOH is described. The reactions are dually promoted by the base in short time (15 min.) at ambient conditions in aqueous medium.

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