122077-86-5 Usage
General Description
1,4-Ethanoquinoxaline,2,3-dihydro-6-methoxy-(9CI) is a chemical compound with the molecular formula C10H12N2O. It is a derivative of ethanoquinoxaline and contains a methoxy group. 1,4-Ethanoquinoxaline,2,3-dihydro-6-methoxy-(9CI) is a heterocyclic organic compound that is commonly used in the pharmaceutical industry for the synthesis of various drugs. It has been studied for its potential biological activities, including its role as an antimicrobial, antifungal, and antiviral agent. Additionally, it has been investigated for its potential use as an antioxidant and for its potential effects on the central nervous system.
Check Digit Verification of cas no
The CAS Registry Mumber 122077-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122077-86:
(8*1)+(7*2)+(6*2)+(5*0)+(4*7)+(3*7)+(2*8)+(1*6)=105
105 % 10 = 5
So 122077-86-5 is a valid CAS Registry Number.
122077-86-5Relevant articles and documents
DIAZABICYCLOALKANES WITH NITROGEN ATOMS IN BRIDGEHEAD POSITIONS. 17. EFFECT OF SUBSTITUENTS IN BENZO-1,4-DIAZABICYCLOOCTENE ON PROTON AFFINITY AND OPENING BY CHLOROFORMATE ESTER
Gall', A. A.,Doronina, S. O.,Shishkin, G. V.,Voityuk, A. A.,Bliznyuk, A. A.
, p. 305 - 310 (1989)
The reaction of benzo-1,4-diazabicyclooctene with chloroformate ester is accompanied by opening of the diazabicyclo fragment and addition of chloroformate ester.A nitro group in the 4' position lowers the rate constant for opening by 40 times in comparison to the unsubstituted heterocycle, while a 4' methoxy group practically does not affect the reaction rate.The ratio of the 6- and 7- substituted 1-(β-chloroethyl)-4-ethoxycarbonyl-1,2,3,4-tetrahydroquinoxalines which are formed agrees with a quantum chemical calculation of the proton affinity and indicates a principally inductive effect of the substituents on the reactivity of the heteroatoms.