796061-07-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(Toluene-4-sulfonylamino)phenylboronic acid, pinacol ester is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to be incorporated into organic molecules through Suzuki-Miyaura cross-coupling reactions. This allows for the creation of new drugs with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(Toluene-4-sulfonylamino)phenylboronic acid, pinacol ester is used as a building block for constructing complex organic molecules. Its reactivity and compatibility with various coupling partners make it a valuable component in the development of novel organic compounds.
Used in Chemical Transformations:
2-(Toluene-4-sulfonylamino)phenylboronic acid, pinacol ester is utilized as a versatile reagent in chemical transformations, enabling the modification of organic compounds to achieve desired properties or functions. Its ability to participate in a range of reactions makes it a valuable tool in the hands of organic chemists.
Check Digit Verification of cas no
The CAS Registry Mumber 796061-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,0,6 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 796061-07:
(8*7)+(7*9)+(6*6)+(5*0)+(4*6)+(3*1)+(2*0)+(1*7)=189
189 % 10 = 9
So 796061-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H24BNO4S/c1-14-10-12-15(13-11-14)26(22,23)21-17-9-7-6-8-16(17)20-24-18(2,3)19(4,5)25-20/h6-13,21H,1-5H3
796061-07-9Relevant academic research and scientific papers
Palladium-Catalyzed Regioselective Synthesis of 3-Arylindoles from N-Ts-Anilines and Styrenes
Youn, So Won,Ko, Tae Yun,Jang, Young Ho
, p. 6636 - 6640 (2017/05/29)
A Pd-catalyzed intermolecular oxidative annulation between N-Ts-anilines and styrenes was developed. This method offers a straightforward and robust approach to a wide range of 3-arylindoles using readily available starting materials with good functional-group tolerance and high regioselectivity and efficiency. Further elaboration of the products obtained from this process provided access to highly functionalized and structurally diverse indoles, for example, 3-(indol-3-yl)carbazoles, 1,9-dihydropyrrolo-[2,3-b]carbazoles, and 3′-aryl-3,5′-biindoles.
Synthesis and reactivity of sulfonamides containing boronate esters
He, Xiao-Feng,Zhang, Haiwen,Vogels, Christopher M.,Decken, Andreas,Westcott, Stephen A.
, p. 369 - 375 (2007/10/03)
Sulfonamides containing pinacol protected boronate ester groups have been prepared by the addition of H2NC6H4Bpin (pin = O2C2Me4) to sulfonyl chlorides p-RC 6H4SO
