850567-21-4 Usage
Uses
Used in Pharmaceutical Industry:
3-(N-Ethylaminocarbonyl)benzeneboronic Acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic properties or improving their stability.
Used in Medical Research:
In the field of medical research, 3-(N-Ethylaminocarbonyl)benzeneboronic Acid may be employed as a tool compound to study the interactions between boronic acids and biological molecules, such as enzymes or receptors. This can provide insights into the development of new therapeutic strategies or the understanding of disease mechanisms.
It is important to handle 3-(N-Ethylaminocarbonyl)benzeneboronic Acid with care, as with any chemical substance, to avoid unfavorable reactions or side-effects.
Check Digit Verification of cas no
The CAS Registry Mumber 850567-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 850567-21:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*7)+(2*2)+(1*1)=174
174 % 10 = 4
So 850567-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H12BNO3/c1-2-11-9(12)7-4-3-5-8(6-7)10(13)14/h3-6,13-14H,2H2,1H3,(H,11,12)
850567-21-4Relevant articles and documents
Noncryogenic I/Br-Mg exchange of aromatic halides bearing sensitive functional groups using i-PrMgCl-Bis[2-(N,N-dimethylamino)ethyl] ether complexes
Wang, Xiao-Jun,Sun, Xiufeng,Zhang, Li,Xu, Yibo,Krishnamurthy, Dhileepkumar,Senanayake, Chris H.
, p. 305 - 307 (2006)
Iodo- and bromoaromatics bearing sensitive carboxylic ester and cyano groups underwent a selective halide-magnesium exchange with isopropylmagnesium chloride at ambient temperature in the presence of bis[2-(N,N-dimethylamino) ethyl] ether to afford the corresponding Grignard reagents. The newly formed reactive Grignard reagents were allowed to react with electrophiles such as trimethylborate to afford arylboronic acids in good to excellent yields.
