443-42-5 Usage
General Description
3,5-Difluoro-4-methoxyphenol is a chemical compound that is also known as 4-methoxy-3,5-difluorophenol. It is an aromatic compound with the molecular formula C7H6F2O2. This chemical is a white solid at room temperature and is soluble in organic solvents such as ethanol and ether. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 3,5-Difluoro-4-methoxyphenol also has antibacterial and antifungal properties, which make it a useful ingredient in some antiseptic and disinfectant products. Additionally, it is also used as a reagent in organic synthesis reactions. Overall, 3,5-Difluoro-4-methoxyphenol is a versatile chemical compound with a range of industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 443-42-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 443-42:
(5*4)+(4*4)+(3*3)+(2*4)+(1*2)=55
55 % 10 = 5
So 443-42-5 is a valid CAS Registry Number.
443-42-5Relevant articles and documents
Rationally Designed Fluorescence .OH Probe with High Sensitivity and Selectivity for Monitoring the Generation of .OH in Iron Autoxidation without Addition of H2O2
Li, Hongyu,Li, Xiaohua,Shi, Wen,Xu, Yanhui,Ma, Huimin
, p. 12830 - 12834 (2018)
The first sensitive fluorescence .OH probe (1) that is capable of monitoring the generation of trace .OH in iron autoxidation is presented. The probe 1 was designed by utilizing both the unique aromatic hydroxylation and the electrop
Synthesis and evaluation of 1,4-naphthoquinone ether derivatives as SmTGR inhibitors and new anti-schistosomal drugs
Johann, Laure,Belorgey, Didier,Huang, Hsin-Hung,Day, Latasha,Chessé, Matthieu,Becker, Katja,Williams, David L.,Davioud-Charvet, Elisabeth
, p. 3199 - 3217 (2015/08/24)
Investigations regarding the chemistry and mechanism of action of 2-methyl-1,4-naphthoquinone (or menadione) derivatives revealed 3-phenoxymethyl menadiones as a novel anti-schistosomal chemical series. These newly synthesized compounds (1-7) and their di
