94525-07-2 Usage
Aromatic rings
Two The compound contains two aromatic rings, which are characterized by their stability and resistance to chemical reactions.
Hexafluoropropane backbone
One The compound has a hexafluoropropane backbone, which is a carbon chain with six fluorine atoms attached to it.
Building block for polymers and plastics
Common 2,2-bis[4-(4-amino-2-trifluoromethylphenoxy)phenyl]hexafluoropropane is commonly used as a building block in the production of various polymers and plastics.
High chemical and thermal stability
Required The compound is particularly useful in applications that require high chemical and thermal stability.
Specialty coatings and adhesives
Potential applications Due to its unique chemical structure and reactivity, the compound has potential applications in the development of specialty coatings and adhesives.
Pharmaceutical and agrochemical synthesis
Key component The compound can be a key component in the synthesis of pharmaceuticals and agrochemicals.
Safety measures
Essential As with any chemical compound, proper handling and safety measures should be followed to minimize potential hazards associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 94525-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,2 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94525-07:
(7*9)+(6*4)+(5*5)+(4*2)+(3*5)+(2*0)+(1*7)=142
142 % 10 = 2
So 94525-07-2 is a valid CAS Registry Number.
94525-07-2Relevant academic research and scientific papers
Preparation method of aromatic diether diamine
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Paragraph 0047-0048; 0051-0064, (2020/05/02)
The invention belongs to the technical field of diamine monomer synthesis, and particularly relates to a preparation method of aromatic diether diamine. The preparation method comprises the followingsteps: mixing bisphenol AF, a halogenated nitrobenzene compound and a catalyst in a solvent, and carrying out an ether forming reaction to obtain an aromatic diether dinitro compound; and carrying outa reduction reaction on the aromatic diether dinitro compound under the action of a catalyst by taking hydrogen as a reducing agent to obtain the aromatic diether diamine. According to the diamine monomer prepared by the preparation method of aromatic diether diamine disclosed by the invention, the white diamine monomer can be obtained on the premise that recrystallization and other purificationmeans are not needed, so that the good conditions are created for preparing downstream products; the yield of the prepared diamine is greater than 92%, and the purity is greater than 99%; and hydrogenis adopted as a reducing agent to replace hydrazine hydrate with high corrosivity, so that the requirements of reduction reaction on equipment and process conditions are reduced.
