89992-52-9 Usage
Uses
Used in Pharmaceutical Industry:
2,3,5,6-Tetrafluorobenzenemethanamine is used as a building block for the synthesis of various pharmaceutical drugs. Its unique structure allows for the creation of new compounds with potential therapeutic applications, making it a valuable asset in drug development.
Used in Agrochemical Industry:
2,3,5,6-Tetrafluorobenzenemethanamine is used as a key component in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the development of effective and targeted products for agricultural use.
Used in Dye and Pigment Production:
2,3,5,6-Tetrafluorobenzenemethanamine is used as a starting material in the synthesis of dyes and pigments. Its fluorinated structure contributes to the color and stability of these products, making it an essential component in their formulation.
Used in Specialty Chemicals:
2,3,5,6-Tetrafluorobenzenemethanamine is used as an intermediate in the production of specialty chemicals, such as those used in coatings, adhesives, and other industrial applications. Its versatility and reactivity make it a valuable component in the synthesis of these complex compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 89992-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89992-52:
(7*8)+(6*9)+(5*9)+(4*9)+(3*2)+(2*5)+(1*2)=209
209 % 10 = 9
So 89992-52-9 is a valid CAS Registry Number.
89992-52-9Relevant academic research and scientific papers
PROCESS FOR PREPARING TETRAFLUOROBENZENE CARBALDEHYDE ALKYL ACETAL
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Page/Page column 20-21; 33, (2008/06/13)
A process for preparing tetrafluorobenzene carbaldehyde alkyl acetal represented by the following formula (II), comprising reducing tetrafluorocyanobenzene represented by the following formula (I) with a metal catalyst containing a platinum group metal in the presence of an alkyl alcohol represented by R-OH (R is an alkyl group of 1 to 4 carbon atoms) and an acid; (I) wherein m is 1 or 2, n is 0 or 1, and m+n is 2, (II) wherein m and n are the same as those in the formula (I), and R is an alkyl group of 1 to 4 carbon atoms.
The pattern of fluorine substitution affects binding affinity in a small library of fluoroaromatic inhibitors for carbonic anhydrase
Doyon, Jeffrey B.,Jain, Ahamindra
, p. 183 - 185 (2008/02/11)
(equation presented) A library of fluoroaromatic inhibitors of carbonic anhydrase has been found to bind in a manner dependent on both hydrophobicity and the pattern of substitution of the fluoroaromatic ring. All of the compounds in the library bind to the protein with Kd 3 nM. We have inferred two distinct binding modes from our data, which suggest two types of interactions that should be considered when designing fluorinated drugs.
