850623-61-9 Usage
General Description
POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is a chemical compound consisting of potassium, fluorine, boron, and butoxyphenyl. It is commonly used as a reagent in organic synthesis for the preparation of various organic compounds. POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE is known for its ability to effectively transfer the butoxyphenyl group to other organic molecules, making it a useful tool for creating new chemical compounds in laboratory settings. It is also utilized in the development of pharmaceuticals, agrochemicals, and materials science due to its versatile reactivity and stability. Overall, POTASSIUM (4-BUTOXYPHENYL)TRIFLUOROBORATE plays an important role in the field of organic chemistry and is a valuable tool for researchers and scientists.
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 articles and documents
The facile and direct formylation of organoboron aromatic compounds with benzodithiolylium tetrafluoroborate
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
