873566-75-7 Usage
General Description
3-Amino-4-fluorophenylboronic acid is a chemical compound with the chemical formula C6H7BNO2F. It is a boronic acid derivative that contains an amino group and a fluorine atom attached to a phenyl ring. 3-Amino-4-fluorophenylboronic acid is commonly used in organic synthesis as a reactant in the formation of carbon-carbon and carbon-nitrogen bonds. It is also used as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 3-Amino-4-fluorophenylboronic acid has been studied for its potential anti-cancer and anti-diabetic properties, making it a compound of interest in medicinal chemistry research. Overall, this chemical compound plays a crucial role in the development of various important products and has potential applications in the fields of medicine and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 873566-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,5,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 873566-75:
(8*8)+(7*7)+(6*3)+(5*5)+(4*6)+(3*6)+(2*7)+(1*5)=217
217 % 10 = 7
So 873566-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7BFNO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,10-11H,9H2
873566-75-7Relevant articles and documents
Synthesis of 3-amino-4-fluorophenylboronic acid method
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Paragraph 0024; 0025; 0030, (2017/02/09)
The invention belongs to the field of synthesis of organic chemicals, and relates to a method for synthesizing 3-amino-4-fluorophenylboronic acid, which comprises the following steps: 1. preparing fluorobromobenzene into a Grignard reagent, and reacting with trimethyl borate to obtain an intermediate fluorophenylboronic acid A; 2. reacting the intermediate A with fuming nitric acid to generate an intermediate 3-nitro-4-fluorophenylboronic acid B; and 3. hydrogenating the intermediate B by using a palladium-on-carbon catalyst to generate the product 3-amino-4-fluorophenylboronic acid C. The synthesis method has the advantages of accessible raw materials and lower cost, is simple to operate, and provides a proper way for preparing 3-amino-4-fluorophenylboronic acid.