956101-10-3 Usage
Uses
Used in Pharmaceutical Research:
2-Chloro-7-fluoroquinazoline is utilized as a key intermediate in the synthesis of novel drugs, targeting various biological processes. Its unique structure allows for the development of compounds with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemicals:
In the agrochemical industry, 2-Chloro-7-fluoroquinazoline is used as a building block for the creation of new pesticides or herbicides. Its chemical versatility aids in the design of effective and environmentally friendly agrochemicals.
Used in Material Science:
2-Chloro-7-fluoroquinazoline is employed in material science for the development of new functional materials. Its reactivity and structural features can be harnessed to produce materials with unique properties for various applications, such as sensors, catalysts, or advanced materials for electronics and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 956101-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,1,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 956101-10:
(8*9)+(7*5)+(6*6)+(5*1)+(4*0)+(3*1)+(2*1)+(1*0)=153
153 % 10 = 3
So 956101-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H4ClFN2/c9-8-11-4-5-1-2-6(10)3-7(5)12-8/h1-4H
956101-10-3Relevant academic research and scientific papers
Eco-efficient one-pot synthesis of quinazoline-2,4(1H,3H)-diones at room temperature in water
Tian, Xin-Chuan,Huang, Xing,Wang, Dan,Gao, Feng
, p. 824 - 829 (2016/10/06)
An efficient one-pot synthesis of quinazoline-2,4(1H,3H)-diones was developed. First, the reactions of anthranilic acid derivatives with potassium cyanate afforded the corresponding urea derivatives. Then, cyclization of the urea derivatives with NaOH afforded the monosodium salts of benzoylene urea. Finally, HCl treatment afforded the desired products in near-quantitative yields. This is an eco-efficient method because all the reactions were carried out in water, and the desired products were obtained simply by filtration. The aqueous filtrate was the only waste generated from the reaction. We scaled up the reaction to 1 kg starting material, thus establishing an alternative approach for the green synthesis of quinazoline-2,4(1H,3H)-diones in the chemical and pharmaceutical industries.
