35295-35-3 Usage
Description
3-(1,1,2,2-TETRAFLUOROETHOXY)BENZALDEHYDE is an organic compound characterized by its unique tetrafluoroethoxy group attached to a benzene ring. 3-(1,1,2,2-TETRAFLUOROETHOXY)BENZALDEHYDE is known for its potential applications in the synthesis of various chemical products, particularly those with fluorinated structures.
Uses
Used in Pharmaceutical Industry:
3-(1,1,2,2-TETRAFLUOROETHOXY)BENZALDEHYDE is used as a key intermediate in the synthesis of novel series of substituted N-[3-(1,1,2,2-tetrafluoroethoxy)benzyl]-N-(3-phenoxyphenyl)-trifluoro-3-amino-2-propanols. These compounds have potential applications in the development of new pharmaceuticals, particularly those targeting specific biological receptors or pathways.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-(1,1,2,2-TETRAFLUOROETHOXY)BENZALDEHYDE serves as a versatile building block for creating a variety of fluorinated organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of specialty chemicals, materials, and other advanced products.
Used in Material Science:
The incorporation of fluorine atoms in the structure of 3-(1,1,2,2-TETRAFLUOROETHOXY)BENZALDEHYDE can lead to materials with enhanced properties, such as increased chemical stability, improved thermal resistance, and reduced surface energy. These characteristics make it a promising candidate for use in the development of advanced materials for various applications, including coatings, lubricants, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 35295-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,9 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35295-35:
(7*3)+(6*5)+(5*2)+(4*9)+(3*5)+(2*3)+(1*5)=123
123 % 10 = 3
So 35295-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F4O2/c10-8(11)9(12,13)15-7-3-1-2-6(4-7)5-14/h1-5,8H
35295-35-3Relevant articles and documents
Substituted N, N-disubstituted diamino compounds useful for inhibiting cholesteryl ester transfer protein activity
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, (2008/06/13)
The invention relates to substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atherosclerosis and other coronary artery diseases. Preferred tertiary-heteroalkylamine compounds are substituted N,N-disubstituted diamines. A preferred specific N,N-disubstituted diamine is the compound:
