86845-35-4 Usage
Uses
Used in Pharmaceutical Industry:
3,3'-BIS(TRIFLUOROMETHYL)DIPHENYLMETHANE is used as a building block or reagent for the synthesis of various organic compounds, including pharmaceuticals. Its high thermal and chemical stability contribute to the development of new drugs with improved properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3,3'-BIS(TRIFLUOROMETHYL)DIPHENYLMETHANE serves as a key component in the synthesis of agrochemicals, enhancing the effectiveness and stability of these compounds for agricultural applications.
Used in Polymer Production:
3,3'-BIS(TRIFLUOROMETHYL)DIPHENYLMETHANE is utilized in the production of polymers, where its stability and solubility in organic solvents contribute to the creation of high-quality polymer materials with specific properties.
Used in Specialty Chemicals:
3,3'-BIS(TRIFLUOROMETHYL)DIPHENYLMETHANE is also used in the synthesis of other specialty chemicals, where its unique characteristics can be leveraged to develop new products with targeted applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 86845-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,4 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86845-35:
(7*8)+(6*6)+(5*8)+(4*4)+(3*5)+(2*3)+(1*5)=174
174 % 10 = 4
So 86845-35-4 is a valid CAS Registry Number.
86845-35-4Relevant academic research and scientific papers
Hypophosphorous acid-iodine: A novel reducing system. Part 2: Reduction of benzhydrols to diarylmethylene derivatives
Gordon, Paul E.,Fry, Albert J.
, p. 831 - 833 (2007/10/03)
A mixture of hypophosphorous acid (H3PO2) and iodine in acetic acid reduces a variety of substituted benzhydrols to the corresponding methylene derivatives in very high yields. The active reducing agent is hydrogen iodide generated by reaction between iodine and hypophosphorous acid.
Carbon Acidity. 66. Equilibrium Ion Pair Acidities of Substituted Diphenylmethanes in Cyclohexylamine
Streitwieser, Andrew Jr.,Vorpagel, Erich R.,Chen, Chia-Chung
, p. 6970 - 6975 (2007/10/02)
The pKCsCHA values are reported for a number of symmetrically meta- and para-substituted diphenylmethanes.The pKCsCHA values for the meta series (Me, 33.8; OMe, 32.7; F, 29.9; CF3, 28.9; Ph, 32.3; H, 33.4) give a normal Hammett plot with ρ = 9.69.The para series (Me, 35.1; OMe,37.6; Ph, 30.8; NMe2, 38.6; SPh, 28.8; CN, 23.0; SO2Me, 22.4) do not fit attempted correlations with ?, the Yukawa-Tsuno modifications, or dual substituent parameter approaches.Electron-donating groups are more anion destabilizing than in other reference systems. "Amphoteric" substituents, those that stabilize both anions and cations (phenyl, thio, etc.), cause special problems in generalized correlations.
