438050-23-8 Usage
Uses
Used in Pharmaceutical Industry:
(4-Ethoxy-2,6-difluorophenyl)methanol is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the presence of fluorine atoms and an ethoxy group, allows for the development of new drugs with improved properties, such as enhanced potency, selectivity, and bioavailability.
Used in Agrochemical Industry:
(4-Ethoxy-2,6-difluorophenyl)methanol is used as an intermediate in the production of agrochemicals, specifically crop protection products. Its chemical structure can be utilized to create new active ingredients for pesticides, herbicides, and other agricultural chemicals, potentially leading to more effective and environmentally friendly solutions for crop protection.
Used in Organic Chemistry Research:
(4-Ethoxy-2,6-difluorophenyl)methanol serves as a valuable building block in the synthesis of more complex organic molecules. Its unique functional groups and structural features make it a versatile component in the development of novel organic compounds for various applications, including materials science, medicinal chemistry, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 438050-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,0,5 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 438050-23:
(8*4)+(7*3)+(6*8)+(5*0)+(4*5)+(3*0)+(2*2)+(1*3)=128
128 % 10 = 8
So 438050-23-8 is a valid CAS Registry Number.
438050-23-8Relevant academic research and scientific papers
Optimization of benzyloxazoles as non-nucleoside inhibitors of HIV-1 reverse transcriptase to enhance Y181C potency
Bollini, Mariela,Gallardo-Macias, Ricardo,Spasov, Krasimir A.,Tirado-Rives, Julian,Anderson, Karen S.,Jorgensen, William L.
, p. 1110 - 1113 (2013/03/14)
Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved activity towards Tyr181Cys containing variants was pursued with the assistance of free energy perturbation (FEP) calculations. Optimization of the 4-R substituent in 1 led to ethyl and isopropyl analogs 1e and 1f with 1-7 nM potency towards both the wild-type virus and a Tyr181C variant.
Novel piperazine derivatives
-
, (2008/06/13)
The present invention is a chemical compound of formula (I) or a pharmaceutically acceptable salts, solvates and esters thereof, wherein R1 to R4, A1, A2 m and n are as described in the specification.
