89992-50-7 Usage
General Description
2,3,5,6-Tetrafluoro-1,4-benzenedimethanamine, also known as tetrafluorophthalimide, is a chemical compound with the molecular formula C6H2F4N2. It is a crystalline solid that is used in the synthesis of pharmaceuticals and agrochemicals. 2,3,5,6-Tetrafluoro-1,4-benzenedimethanamine is known for its ability to react with various chemicals and form strong, stable bonds, making it a valuable building block for the creation of complex organic molecules. Additionally, it is used as a reagent in the production of dyes and pigments, as well as a catalyst in polymerization reactions. However, it is important to handle this chemical with care, as prolonged exposure to high concentrations of 2,3,5,6-Tetrafluoro-1,4-benzenedimethanamine can be harmful to human health.
Check Digit Verification of cas no
The CAS Registry Mumber 89992-50-7 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 89992-50:
(7*8)+(6*9)+(5*9)+(4*9)+(3*2)+(2*5)+(1*0)=207
207 % 10 = 7
So 89992-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F4N2/c9-5-3(1-13)6(10)8(12)4(2-14)7(5)11/h1-2,13-14H2
89992-50-7Relevant articles and documents
Synthesis, structure, and photoreactions of fluorinated 2,11-diaza[32]paracyclophane: Photochemical formation of cage-diene type benzene dimer
Okamoto, Hideki,Kozai, Tetsuya,Okabayashi, Zenji,Shinmyozu, Teruo,Ota, Hiromi,Amimoto, Kiichi,Satake, Kyosuke
, (2017)
An octafluorinated 2,11-diaza[32]paracyclophane derivative 12 was prepared, and its photochemical reaction was investigated. Upon irradiation at 300?nm, the fluorinated azacyclophane 12 underwent efficient photodimerization of the benzene cores to afford the corresponding photoisomer 13, which possessed cage diene benzene dimer structure (pentacyclo[6.4.0.0.2,70.3,1206,9]dodeca-4,10-diene skeleton). The cage diene structure was established by single-crystal X-ray diffraction analysis. The cage diene 13 thermally isomerized to a syn-o,o′-dibenzene isomer 22. The activation parameters for the thermal isomerization were determined to be Ea?=?121?kJ?mol?1, ΔH≠?=?118?kJ?mol?1, ΔS≠ (293?K)?=?22?J?mol?1?K?1, and ΔG≠ (293?K)?=?111?kJ?mol?1. It was revealed that, by photoirradiation at 300?nm, the syn-o,o′-dibenzene isomer 22 underwent facile intramolecular [π4s?+?π4s] cycloaddition to reproduce the cage diene isomer 13.