256658-04-5 Usage
Uses
Used in Pharmaceutical Development:
5-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-2-FURALDEHYDE is used as a versatile building block in the pharmaceutical industry for the development of new drugs. Its unique structure allows it to be a key intermediate in the synthesis of a variety of organic compounds with potential medicinal applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-2-FURALDEHYDE is utilized as a valuable intermediate for the synthesis of various agrochemicals. Its strong electron-withdrawing trifluoromethyl groups contribute to the creation of effective compounds for agricultural use.
Used in Materials Science:
5-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-2-FURALDEHYDE is employed as a component in materials science for the development of new materials with specific properties. Its structural features make it suitable for creating materials with tailored characteristics for various applications.
Used in Organic Electronics:
In the field of organic electronics, 5-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-2-FURALDEHYDE is used as a component in the design and synthesis of organic electronic devices. Its properties make it a promising candidate for enhancing the performance of these devices.
Used in Optoelectronics:
5-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-2-FURALDEHYDE also has potential applications in the field of optoelectronics, where it can be used to develop new optoelectronic devices and materials. Its unique structure and properties contribute to the advancement of technology in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 256658-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,6,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 256658-04:
(8*2)+(7*5)+(6*6)+(5*6)+(4*5)+(3*8)+(2*0)+(1*4)=165
165 % 10 = 5
So 256658-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H6F6O2/c14-12(15,16)8-3-7(4-9(5-8)13(17,18)19)11-2-1-10(6-20)21-11/h1-6H
256658-04-5Relevant articles and documents
The Influence of Substitution on Thiol-Induced Oxanorbornadiene Fragmentation
De Pascalis, Lucrezia,Yau, Mei-Kwan,Svatunek, Dennis,Tan, Zhuoting,Tekkam, Srinivas,Houk,Finn
supporting information, p. 3751 - 3754 (2021/05/10)
Oxanorbornadienes (ONDs) undergo facile Michael addition with thiols and then fragment by a retro-Diels-Alder (rDA) reaction, a unique two-step sequence among electrophilic cleavable linkages. The rDA reaction rate was explored as a function of the furan
HETEROCYCLIC COMPOUND
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Page/Page column 74-75, (2011/04/18)
The present invention relates to a compound represented by wherein each symbol is as defined in the specification, a salt thereof and the like.
HETEROCYCLIC COMPOUND
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Page/Page column 54, (2011/10/19)
The present invention relates to a compound represented by wherein each symbol is as defined in the specification, a salt thereof and the like.