116412-99-8 Usage
Description
4’-trifluoromethyl-3,4-dimethoxybenzophenone is a chemical compound that features a benzophenone core with a trifluoromethyl group at the 4' position and methoxy groups at the 3 and 4 positions on the phenyl rings. 4’-trifluoromethyl-3,4-dimethoxybenzophenone is known for its potential applications in various chemical and pharmaceutical processes due to its unique structural features.
Uses
Used in Pharmaceutical Industry:
4’-trifluoromethyl-3,4-dimethoxybenzophenone is used as a reagent for the preparation of benzophenones, which serve as intermediates in the synthesis of fungicides. Its specific structural attributes, including the trifluoromethyl group, can enhance the bioactivity and effectiveness of the resulting fungicides, making it a valuable component in the development of new antifungal agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4’-trifluoromethyl-3,4-dimethoxybenzophenone can be utilized as a building block for the creation of more complex organic molecules. Its presence in a molecule can influence the molecule's reactivity, stability, and other properties, which can be advantageous in the synthesis of various target compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 116412-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116412-99:
(8*1)+(7*1)+(6*6)+(5*4)+(4*1)+(3*2)+(2*9)+(1*9)=108
108 % 10 = 8
So 116412-99-8 is a valid CAS Registry Number.
116412-99-8Relevant articles and documents
Synthesis of two new naphthalene-containing compounds and their bindings to human serum albumin
Wang, Xia,Xing, Yue,Su, Jing,Wang, Changsheng,Wang, Zishi,Yu, Yinghui,Xu, Hongliang,Ma, DongSheng
, p. 3435 - 3448 (2020/07/04)
Two naphthalene-containing compounds, 4-hydroxy-6,7-dimethoxy-1-(4-(trifluoromethyl)phenyl)-2-naphthoic acid (A) and 4-hydroxy-6,7-dimethoxy-1-phenyl-2-naphthoic acid (B), were prepared by several steps. Their bindings to human serum albumin (HSA) were st
PHOTOCHROMIC MATERIALS DEMONSTRATING IMPROVED FADE RATES
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Page/Page column 15, (2008/06/13)
Various photochromic materials are provided that are essentially free of polymerizable unsaturated groups, and comprise: a) an indeno[2′,3′:3,4]naphtho[1,2-b]pyran; and b) an electron-withdrawing, non-conjugating group bonded at the 11-position of the indeno[2′,3′:3,4]naphtho[1,2-b]pyran. Alternative embodiments include various substituents at other positions of the indeno[2′,3′:3,4]naphtho[1,2-b]pyran. Also provided are photochromic articles including a substrate and one of the above photochromic materials, in contact with at least a portion of the substrate.
