850623-61-9 Usage
Uses
Used in Organic Synthesis:
POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is used as a reagent for the preparation of various organic compounds due to its ability to effectively transfer the butoxyphenyl group to other molecules, facilitating the creation of new chemical compounds in laboratory settings.
Used in Pharmaceutical Development:
In the pharmaceutical industry, POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is used as a key intermediate in the synthesis of drug molecules, contributing to the development of new medications with potential therapeutic applications.
Used in Agrochemical Development:
POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is utilized as a reagent in the synthesis of agrochemicals, aiding in the development of new compounds for agricultural applications such as pesticides and herbicides.
Used in Materials Science:
In the field of materials science, POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is employed in the synthesis of novel materials with specific properties, such as improved stability or reactivity, for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 850623-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,6,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 850623-61:
(8*8)+(7*5)+(6*0)+(5*6)+(4*2)+(3*3)+(2*6)+(1*1)=159
159 % 10 = 9
So 850623-61-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BF3O.K/c1-2-3-8-15-10-6-4-9(5-7-10)11(12,13)14;/h4-7H,2-3,8H2,1H3;/q-1;+1
850623-61-9Relevant academic research and scientific papers
Petruzziello, Diego,Gualandi, Andrea,Jaffar, Hamza,Lopez-Carrillo, Veronica,Cozzi, Pier Giorgio
, p. 4909 - 4917 (2013)
Organoboron compounds can be used to effect a direct formylation in the absence of transition metals. We report that the direct reaction between boronic derivatives and benzodithiolylium tetrafluoroborate, a commercially available carbenium ionic compound, is possible and provides access to many interesting compounds without the use of transition metals. The direct reaction of the carbenium ion with boronic derivatives results in the formation of substituted arylcarbenium ions, a number of which can be further utilized in materials chemistry or for the direct transformation into other compounds. In addition to the rich chameleonic chemical nature of the benzodithiol intermediate, such species can also undergo a metallation reaction and subsequent treatment with a wide range of electrophiles to access a variety of functional groups (aldehyde, ketone, acid, and alkyl groups). Copyright
