876189-19-4 Usage
Uses
Used in Organic Synthesis:
4-Methoxycarbonyl-3,5-dimethylphenylboronic acid is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a versatile component in the synthesis of complex organic molecules.
Used in Drug Discovery:
4-Methoxycarbonyl-3,5-dimethylphenylboronic acid is used as a valuable tool in drug discovery due to its ability to form stable complexes with diols. This property allows for the development of new chemical reactions and the exploration of potential drug candidates with improved efficacy and selectivity.
Used in High-Throughput Screening:
4-Methoxycarbonyl-3,5-dimethylphenylboronic acid is utilized in the construction of small molecule libraries for high-throughput screening in drug development. Its presence in these libraries enables the rapid identification of promising drug candidates with potential therapeutic applications.
Used in Medicinal Chemistry:
As an important chemical reagent, 4-Methoxycarbonyl-3,5-dimethylphenylboronic acid is used in medicinal chemistry for the design and synthesis of novel therapeutic agents. Its unique properties and reactivity contribute to the development of innovative drugs with improved pharmacological profiles.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, 4-Methoxycarbonyl-3,5-dimethylphenylboronic acid is employed for the synthesis of a wide range of organic compounds. Its versatility and reactivity make it a valuable component in the development of new synthetic routes and methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 876189-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,1,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 876189-19:
(8*8)+(7*7)+(6*6)+(5*1)+(4*8)+(3*9)+(2*1)+(1*9)=224
224 % 10 = 4
So 876189-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BO4/c1-6-4-8(11(13)14)5-7(2)9(6)10(12)15-3/h4-5,13-14H,1-3H3
876189-19-4Relevant academic research and scientific papers
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 (2007/10/03)
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.
