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(3R,5S)-1-(2-Fluoro-4-nitrophenyl)-3,5-dimethylpiperazine is a chiral chemical compound with the molecular formula C11H15FN4O2. It is a derivative of piperazine, featuring a 2-fluoro-4-nitrophenyl group attached to the piperazine ring, along with two methyl groups at the 3rd and 5th positions. The specific configuration of the piperazine and methyl groups endows (3R,5S)-1-(2-Fluoro-4-nitrophenyl)-3,5-dimethylpiperazine with unique structural and potentially beneficial properties, making it a candidate for pharmaceutical research and drug development.

866538-93-4

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866538-93-4 Usage

Uses

Used in Pharmaceutical Research:
(3R,5S)-1-(2-Fluoro-4-nitrophenyl)-3,5-dimethylpiperazine is used as a research compound for exploring its potential applications in the development of new pharmaceuticals. Its unique structure and properties may offer advantages in the treatment of various diseases and conditions.
Used in Drug Development:
In the pharmaceutical industry, (3R,5S)-1-(2-Fluoro-4-nitrophenyl)-3,5-dimethylpiperazine is utilized as a lead compound in the design and synthesis of novel drugs. Its specific configuration and functional groups may contribute to the discovery of new therapeutic agents with improved efficacy and selectivity.
Further studies are required to determine the specific uses and potential benefits of (3R,5S)-1-(2-Fluoro-4-nitrophenyl)-3,5-dimethylpiperazine in various applications. Its unique structure and properties may pave the way for innovative solutions in the field of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 866538-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,5,3 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 866538-93:
(8*8)+(7*6)+(6*6)+(5*5)+(4*3)+(3*8)+(2*9)+(1*3)=224
224 % 10 = 4
So 866538-93-4 is a valid CAS Registry Number.

866538-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-fluoro-4-nitrophenyl)-3,5-dimethylpiperazine

1.2 Other means of identification

Product number -
Other names (3R,5S)-1-(2-FLUORO-4-NITROPHENYL)-3,5-DIMETHYLPIPERAZINE

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:866538-93-4 SDS

866538-93-4Relevant academic research and scientific papers

Thiazolidine derivatives or salts thereof as an active ingredient an inhibitor Pim

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Paragraph 0702; 0703, (2018/10/19)

PROBLEM TO BE SOLVED: To provide compounds which have excellent Pim inhibitory action and are useful as pharmaceuticals.SOLUTION: A compound is a thiazolidine derivative represented by the general formula (1) in the figure, or a salt thereof. (In the formula, X represents O or S; Rrepresents a hydrogen atom or a Calkyl group; Z, Z, Z, Z, Zand Zeach independently represent CH or N; Y represents an optionally substituted, divalent Caromatic hydrocarbon group or the like; Am represents a disubstituted amino group, or an optionally substituted, nitrogen-containing saturated heterocyclic group; and Rand Reach independently represent a hydrogen atom, a halogen atom, an alkyl group or the like.)

TRIAZOLOPYRIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE and INFLAMMATORY DISEASES

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Page/Page column 84, (2008/12/06)

Novel triazolopyridine compounds are disclosed that have a formula represented by Formula (I). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non- limiting example, ECM degradation, joint degradation and/or inflammation, and others.

Synthesis and SAR of novel oxazolidinones: Discovery of ranbezolid

Das, Biswajit,Rudra, Sonali,Yadav, Ajay,Ray, Abhijit,Raja Rao,Srinivas,Soni, Ajay,Saini, Suman,Shukla, Shalini,Pandya, Manisha,Bhateja, Pragya,Malhotra, Sunita,Mathur, Tarun,Arora,Rattan, Ashok,Mehta, Anita

, p. 4261 - 4267 (2007/10/03)

Novel oxazolidinones were synthesized containing a number of substituted five-membered heterocycles attached to the 'piperazinyl-phenyl-oxazolidinone' core of eperezolid. Further, the piperazine ring of the core was replaced by other diamino-heterocycles.

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