850568-12-6 Usage
Uses
Used in Chemical Research:
4-(N-Ethylaminocarbonyl)phenylboronic Acid is used as a reagent in chemical research for its ability to form stable covalent bonds with other compounds. Its stability and reactivity make it a valuable tool in exploring various chemical interactions and reactions.
Used in Organic Chemistry:
In the field of organic chemistry, 4-(N-Ethylaminocarbonyl)phenylboronic Acid is utilized as a reagent to facilitate a range of chemical reactions. Its unique properties allow it to participate in various interactions, making it a versatile compound for researchers to study and develop new organic compounds and reactions.
Used in Laboratory Settings:
4-(N-Ethylaminocarbonyl)phenylboronic Acid is commonly used in laboratory settings for its potential applications in a variety of chemical processes. Its reactivity and stability make it an essential component in the development and testing of new chemical compounds and reactions.
Used in the Synthesis of Pharmaceuticals and Bioactive Compounds:
Due to its ability to form stable covalent bonds, 4-(N-Ethylaminocarbonyl)phenylboronic Acid can be used as a reagent in the synthesis of pharmaceuticals and bioactive compounds. Its unique properties allow it to participate in various chemical reactions, making it a valuable tool in the development of new drugs and therapeutic agents.
Used in Material Science:
In material science, 4-(N-Ethylaminocarbonyl)phenylboronic Acid can be employed as a reagent to develop new materials with specific properties. Its ability to form stable covalent bonds can be utilized to create materials with enhanced characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 850568-12-6 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 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850568-12:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*8)+(2*1)+(1*2)=176
176 % 10 = 6
So 850568-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H12BNO3/c1-2-11-9(12)7-3-5-8(6-4-7)10(13)14/h3-6,13-14H,2H2,1H3,(H,11,12)
850568-12-6Relevant articles and documents
Carboxylic acid recognition of an N-ethyl-substituted diamidine having a diphenylnaphthalene unit in competing protic solvents
Hoshihara, Yuki,Kusukawa, Takahiro,Matoba, Keisuke,Nakajima, Akane,Tanaka, Syugo
, (2021/08/13)
A new diphenylnaphthalene-based diamidine (1) having an N-ethyl-substituent to improve its solubility has been designed and synthesized for the recognition of dicarboxylic acids. The diamidine 1 forms 1:1 complexes with the α,ω-dicarboxylic acids in the competing protic solvent, MeOH, using the charge-assisted hydrogen bonding (i.e., formation of amidinium-carboxylate), and the formation of the complexes was determined by 1H NMR and DOSY NMR spectroscopies in a high concentration (2.0 mM). However, at a low concentration (25 μM), the turn-on fluorescence detection of the dicarboxylic acids was not successful because the diamidine 1 emits in MeOH before recognizing the carboxylic acids. Interestingly, the diamidine 1 does not emit in 2-propanaol before recognizing the α,ω-dicarboxylic acids, and succeeded in the detection of a dicarboxylic acid (turn-on response) in the protic solvent, 2-propanol. The interesting tight binding of the diamidine 1 with α,ω-dicarboxylic acids was observed in 2-propanol-d8 using 1H NMR and the restriction of the rotation of the phenyl rings of the 1,8- diphenylnaphthalene unit was also observed. These fluorescence and binding characteristics of the N-ethyl-substituted diamidine 1 are applicable for the detection of carboxylic acids in a protic solvent.
