881811-83-2 Usage
Uses
Used in Pharmaceutical Research:
4-Diphenyl-1-naphthalene boronic acid is used as a key component in Suzuki-Miyaura coupling reactions, which are essential for constructing complex organic molecules. This reaction forms a carbon-carbon bond by coupling a boronic acid with an aryl or vinyl halide, making it a valuable tool in the synthesis of pharmaceutical compounds.
Used in Detection and Quantitation of Carbohydrates:
Due to its boronic acid component, 4-diphenyl-1-naphthalene boronic acid is used as a reagent for the detection and quantitation of carbohydrates in biological systems. It reacts with diols, which are commonly found in sugars, allowing for the identification and measurement of these important biomolecules in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 881811-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,8,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 881811-83:
(8*8)+(7*8)+(6*1)+(5*8)+(4*1)+(3*1)+(2*8)+(1*3)=192
192 % 10 = 2
So 881811-83-2 is a valid CAS Registry Number.
881811-83-2Relevant academic research and scientific papers
Asymmetric Strecker reaction of aldimines using aqueous potassium cyanide by phase-transfer catalysis of chiral quaternary ammonium salts with a tetranaphthyl backbone
Ooi, Takashi,Uematsu, Yukitaka,Maruoka, Keiji
, p. 2548 - 2549 (2007/10/03)
The phase-transfer-catalyzed, highly enantioselective cyanation of aldimines using aqueous KCN has been realized based on the molecular design of chiral quaternary ammonium iodide 2c bearing a stereochemically defined tetranaphthyl backbone. For example,
