6628-93-9 Usage
Description
4-(phenylamino)quinolin-2(1H)-one is a chemical compound with the molecular formula C18H13N2O. It is a derivative of quinolinone, a heterocyclic organic compound. 4-(phenylamino)quinolin-2(1H)-one is a yellowish crystalline solid that is sparingly soluble in water but more soluble in organic solvents. Its structure and properties make it a versatile intermediate in organic chemistry, allowing for the creation of a wide range of compounds with diverse applications.
Uses
Used in Pharmaceutical Industry:
4-(phenylamino)quinolin-2(1H)-one is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and properties enable the development of compounds with potential therapeutic applications, contributing to the advancement of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(phenylamino)quinolin-2(1H)-one is utilized as a key intermediate in the synthesis of agrochemicals. Its versatility in organic chemistry facilitates the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural products to improve crop yields and protect plants from pests and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 6628-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6628-93:
(6*6)+(5*6)+(4*2)+(3*8)+(2*9)+(1*3)=119
119 % 10 = 9
So 6628-93-9 is a valid CAS Registry Number.
6628-93-9Relevant articles and documents
Synthesis and anticancer evaluation of certain indolo[2,3-b]quinoline derivatives
Chen, Yeh-Long,Hung, Hsien-Ming,Lu, Chih-Ming,Li, Kuang-Chieh,Tzeng, Cherng-Chyi
, p. 6539 - 6546 (2007/10/03)
The present report describes the synthesis and anticancer evaluation of certain 11-substituted 6H-indolo[2,3-b]quinolines and their methylated derivatives. These 6H-indolo[2,3-b]quinoline derivatives 11-13 were prepared from the commercially available 1,4