83566-27-2 Usage
General Description
2(1H)-Quinoxalinone,3-amino-7-methyl-(9CI) is a chemical compound with the molecular formula C10H10N2O. It belongs to the quinoxaline family and contains an amino group and a methyl group. 2(1H)-Quinoxalinone,3-amino-7-methyl-(9CI) has various potential biological activities which make it a subject of interest in pharmaceutical research. It has been studied for its potential applications in drug development, particularly as a building block for developing new pharmaceutical compounds with therapeutic properties. Additionally, it has been investigated for its potential use in the field of organic electronics, as a material for organic light-emitting devices and semiconductors. Overall, 2(1H)-Quinoxalinone,3-amino-7-methyl-(9CI) is a versatile compound with potential applications in both pharmaceutical and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 83566-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,6 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83566-27:
(7*8)+(6*3)+(5*5)+(4*6)+(3*6)+(2*2)+(1*7)=152
152 % 10 = 2
So 83566-27-2 is a valid CAS Registry Number.
83566-27-2Relevant articles and documents
Regioselectivity in preparation of unsymmetrically substituted 3-aminoquinoxalin-2(1H)-ones
Csikos, Eva,Goenczi, Csaba,Podanyi, Benjamin,Toth, Gabor,Hermecz, Istvan
, p. 1789 - 1793 (2007/10/03)
Regioisomer formation has to be considered in the preparation of quinoxalines having different substituents at the 2- and 3-position. Oxalomonoimidic acid dimethyl ester or oxalompnoimidic acid diethyl ester, chloro(methyl- , imino)acetic acid ethyl ester, chloro[(Z)-hydroxyimino]acetic acid ethyl ester and (Z)-2-[(E)-hydroxyimino]acetohydroximoyl chloride were applied to the synthesis of 3-aminoquinoxalin-2(1H)-one derivatives, and the isomer ratio was investigated concerning the reactivity of the ring-closure reagent. The structures of reaction products . were identified using 1H, 13C and 15N NMR techniques. A direct synthesis of quinoxaline-2,3(1H,4H)-dione 3-oximes is described.
HETEROCYCLIC SYNTHESIS USING ETHYL CARBOETHOXYFORMIMIDATE
McKillop, Alexander,Henderson, Alan,Ray, Partha S.,Avendano, Carmen,Molinero, Encarnacion G.
, p. 3357 - 3360 (2007/10/02)
Ethyl carboethoxyformimidate is shown to be a versatile reagent for the synthesis of a variety of mono- and bicyclic heterocyclic systems.
