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rel-2-[4-[[(4R,5S)-4,5-Bis(4-chlorophenyl)-2-[4-(1,1-dimethylethyl)-2-ethoxyphenyl]-4,5-dihydro-4,5-dimethyl-1H-imidazol-1-yl]carbonyl]-1-piperazinyl]-1-(4-morpholinyl)ethanone is a complex organic compound with a unique structure that features various functional groups, including piperazinyl, morpholinyl, and a carbonyl group connected to an imidazol-1-yl group. The presence of chloro-substituted phenyl groups and an ethoxy group suggests that rel-2-[4-[[(4R,5S)-4,5-Bis(4-chlorophenyl)-2-[4-(1,1-dimethylethyl)-2-ethoxyphenyl]-4,5-dihydro-4,5-dimethyl-1H-imidazol-1-yl]carbonyl]-1-piperazinyl]-1-(4-morpholinyl)ethanone may possess specific pharmaceutical or biological activities. Its complex structure makes it a potentially interesting target for medical research, although further analysis and studies are required to determine its exact properties and potential applications.

939983-14-9

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939983-14-9 Usage

Uses

Used in Pharmaceutical Industry:
rel-2-[4-[[(4R,5S)-4,5-Bis(4-chlorophenyl)-2-[4-(1,1-dimethylethyl)-2-ethoxyphenyl]-4,5-dihydro-4,5-dimethyl-1H-imidazol-1-yl]carbonyl]-1-piperazinyl]-1-(4-morpholinyl)ethanone is used as a potential pharmaceutical candidate for [specific medical condition or application] due to its complex structure and the presence of various functional groups that may exhibit specific biological activities.
Used in Research and Development:
In the field of chemical research and development, rel-2-[4-[[(4R,5S)-4,5-Bis(4-chlorophenyl)-2-[4-(1,1-dimethylethyl)-2-ethoxyphenyl]-4,5-dihydro-4,5-dimethyl-1H-imidazol-1-yl]carbonyl]-1-piperazinyl]-1-(4-morpholinyl)ethanone serves as a valuable compound for studying its chemical properties, synthesis methods, and potential applications in various fields, including medicine, materials science, and environmental science.

Check Digit Verification of cas no

The CAS Registry Mumber 939983-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,9,8 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 939983-14:
(8*9)+(7*3)+(6*9)+(5*9)+(4*8)+(3*3)+(2*1)+(1*4)=239
239 % 10 = 9
So 939983-14-9 is a valid CAS Registry Number.

939983-14-9SDS

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 2-[4-[(4R,5S)-2-(4-tert-butyl-2-ethoxyphenyl)-4,5-bis(4-chlorophenyl)-4,5-dimethylimidazole-1-carbonyl]piperazin-1-yl]-1-morpholin-4-ylethanone

1.2 Other means of identification

Product number -
Other names 2-(4-((4R,5S)-2-(4-(tert-Butyl)-2-ethoxyphenyl)-4,5-bis(4-chlorophenyl)-4,5-dimethyl-4,5-dihydro-1H-imidazole-1-carbonyl)piperazin-1-yl)-1-morpholinoethanone

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:939983-14-9 SDS

939983-14-9Downstream Products

939983-14-9Relevant academic research and scientific papers

Discovery of RG7112: A small-molecule MDM2 inhibitor in clinical development

Vu, Binh,Wovkulich, Peter,Pizzolato, Giacomo,Lovey, Allen,Ding, Qingjie,Jiang, Nan,Liu, Jin-Jun,Zhao, Chunlin,Glenn, Kelli,Wen, Yang,Tovar, Christian,Packman, Kathryn,Vassilev, Lyubomir,Graves, Bradford

, p. 466 - 469 (2013/07/11)

The p53 tumor suppressor is a potent transcription factor that plays a key role in the regulation of cellular responses to stress. It is controlled by its negative regulator MDM2, which binds directly to p53 and inhibits its transcriptional activity. MDM2

4,4,5,5, Tetrasubstituted imidazolines

-

Page/Page column 14/1, (2008/06/13)

There is provided a compound of formula I and the pharmaceutically acceptable salts and esters thereof wherein X1, X2, R1, R2, R3, R4, R5 and R6 are herein described. The compounds exhibit activity as anticancer agents.

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