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(S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid is a complex chemical compound with multiple component structures. It contains several moieties, including a trifluoromethyl group attached to a phenyl group, a secondary amine, an ether link, a butene moiety, and another phenyl ring. (S)-1-((R)-1-(3,5-bis(trifluoroMethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-aMine Maleic acid is an enantiopure chemical, with the configuration indicated by the 'S-' and 'R-' prefixes in its name. The term "maleic acid" at the end suggests that (S)-1-((R)-1-(3,5-bis(trifluoroMethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-aMine Maleic acid forms a salt or a complex with maleic acid, a di-carboxylic acid. As with other fluorinated compounds, it may exhibit high thermal and chemical stability, making it a candidate for various applications.

1214741-14-6

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  • High purity (alphaS)-alpha-[[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]methyl]-alpha-ethenylbenzenemethanamine monomaleate CAS No.:1214741-14-6

    Cas No: 1214741-14-6

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  • (alphaS)-alpha-[[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]methyl]-alpha-ethenylbenzenemethanamine monomaleate

    Cas No: 1214741-14-6

  • USD $ 1.2-5.0 / Kiloliter

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1214741-14-6 Usage

Uses

Used in Pharmaceutical Industry:
(S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid is used as a potential pharmaceutical compound for its unique structural features. The presence of fluorine atoms and the complex arrangement of functional groups may contribute to its properties, such as high thermal and chemical stability, which are desirable in drug development.
Used in Chemical Research:
(S)-1-((R)-1-(3,5-bis(trifluoroMethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-aMine Maleic acid is used as a research tool in the field of organic chemistry, particularly for studying the effects of fluorination and the behavior of complex molecular structures. Its enantiopurity and the presence of maleic acid may also be of interest in asymmetric synthesis and the development of chiral catalysts.
Used in Material Science:
(S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid may be utilized in the development of new materials with specific properties, such as high thermal stability or unique electronic characteristics, due to its fluorinated and aromatic components.

Check Digit Verification of cas no

The CAS Registry Mumber 1214741-14-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1214741-14:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*4)+(3*1)+(2*1)+(1*4)=116
116 % 10 = 6
So 1214741-14-6 is a valid CAS Registry Number.

1214741-14-6SDS

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 (αS)-α-[[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]methyl]-α-ethenylbenzenemethanamine maleate

1.2 Other means of identification

Product number -
Other names (alphaS)-alpha-[[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]methyl]-alpha-ethenylbenzenemethanamine monomaleate

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:1214741-14-6 SDS

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