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(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl, also known as N-ethyl-1-(3,5-bis(trifluoromethyl)phenyl)propan-2-amine, is a chiral amine compound with the molecular formula C14H16F6N. It features a single chiral center, leading to the existence of two enantiomers, (S)and (R)-isomers. (S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is prominently utilized in pharmaceutical research and drug development, particularly within the realm of medicinal chemistry. It has demonstrated potential biological activities and has shown promise across a spectrum of therapeutic applications. Furthermore, its chemical structure and functional groups render it an ideal candidate for additional chemical modifications and structure-activity relationship studies in the fields of drug design and discovery.

672906-75-1

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672906-75-1 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential biological activities and therapeutic applications. Its unique chemical structure and functional groups allow for further chemical modifications, making it a versatile building block in drug design and discovery.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is employed as a valuable compound for exploring structure-activity relationships. Its chiral nature and potential biological activities make it a promising candidate for the development of novel therapeutic agents.
Used in Chemical Modifications and Structure-Activity Relationship Studies:
(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is utilized as a starting material for chemical modifications and structure-activity relationship studies. Its functional groups and chiral center enable researchers to investigate the effects of structural changes on the compound's biological activities and therapeutic potential.
Used in Drug Design:
(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is used as a component in drug design, where its unique properties and potential for further modification contribute to the development of new and improved pharmaceutical agents.
Used in Discovery of Novel Therapeutic Agents:
(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl is also used in the discovery of novel therapeutic agents, as its potential biological activities and chiral nature make it a valuable tool for identifying new treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 672906-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,9,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 672906-75:
(8*6)+(7*7)+(6*2)+(5*9)+(4*0)+(3*6)+(2*7)+(1*5)=191
191 % 10 = 1
So 672906-75-1 is a valid CAS Registry Number.

672906-75-1Upstream product

672906-75-1Downstream Products

672906-75-1Relevant academic research and scientific papers

OPTICALLY ACTIVE 1-(FLUORO-,TRIFLUOROMETHYL-OR TRIFLUOROMETHOXY-SUBSTITUTED PHENYL)ALKYLAMINE N-MONOALKYL DERIVATIVES AND PROCESS FOR PRODUCING SAME

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Page 60-61, (2010/02/06)

An optically active 1-(fluoro-, trifluoromethyl- or trifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivative represented by the formula [4] is produced by a process including (a) reacting an optically active secondary amine, represented by th

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