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6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is a chromenone derivative with the molecular formula C20H14F3O3. It is characterized by the presence of a trifluoromethyl group and a hydroxy group, which may contribute to its potential pharmaceutical applications. The trifluoromethyl group is known to enhance the biological activity and metabolic stability of pharmaceutical compounds, making this chemical a promising candidate for drug development. Its unique structure and reactivity also make it useful for the synthesis of other organic compounds with similar properties.

105258-37-5

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105258-37-5 Usage

Uses

Used in Pharmaceutical Applications:
6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is used as a potential pharmaceutical candidate due to its structural features that can affect its biological activity and interactions with biological systems. The presence of the trifluoromethyl group may enhance its biological activity and metabolic stability, making it a promising compound for drug development.
Used in Organic Synthesis:
6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is used as a building block in the synthesis of other organic compounds with similar properties. Its unique structure and reactivity make it a valuable component in the development of new chemical entities with potential applications in various fields.
Used in Drug Development:
6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is used as a starting material for the development of new drugs. Its structural features and potential biological activity make it a valuable compound for further research and development in the pharmaceutical industry.
Used in Medicinal Chemistry Research:
6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is used as a subject of study in medicinal chemistry research. Its unique properties and potential applications make it an interesting compound for researchers to explore its therapeutic potential and optimize its properties for specific medical uses.
Used in Chemical Biology:
6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one is used in chemical biology to investigate its interactions with biological systems and understand its potential as a modulator of biological processes. Its structural features may provide insights into the design of new compounds with improved biological activity and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 105258-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,5 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105258-37:
(8*1)+(7*0)+(6*5)+(5*2)+(4*5)+(3*8)+(2*3)+(1*7)=105
105 % 10 = 5
So 105258-37-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H13F3O3/c1-2-10-8-12-14(9-13(10)22)24-17(18(19,20)21)15(16(12)23)11-6-4-3-5-7-11/h3-9,22H,2H2,1H3

105258-37-5SDS

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 6-ethyl-7-hydroxy-3-phenyl-2-(trifluoromethyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 6-Ethyl-7-hydroxy-3-phenyl-2-trifluoromethyl-chromen-4-one

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 -
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More Details:105258-37-5 SDS

105258-37-5Relevant academic research and scientific papers

SYNTHESIS OF ANALOGS OF NATURAL ISOFLAVONES FROM 2,4-DIHYDROXYDEOXYBENZOINS

Luk'yanchikov, M. S.,Khilya, V. P.,Kazakov, A. L.

, p. 740 - 743 (2007/10/02)

A number of analogs of natural isoflavones have been synthesized.The starting materials were 2,4-dihydroxydeoxybenzoins obtained under modified conditions of the Houben-Hoesch reaction.The yields of the isoflavones synthesized were 63-69percent.All the an

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