62686-14-0 Usage
Type of compound
Polycyclic aromatic hydrocarbon
Structure
Two benzene rings fused to a phenazine ring, with a trifluoromethyl group attached to one of the benzene rings
Physical appearance
Pale yellow crystalline solid
Solubility
Insoluble in water, soluble in organic solvents
Potential applications
Organic electronics and materials science
Unique features
Unique structure and electronic properties
Precautions
Trifluoromethyl group may pose health and environmental risks if not managed properly
Check Digit Verification of cas no
The CAS Registry Mumber 62686-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,8 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62686-14:
(7*6)+(6*2)+(5*6)+(4*8)+(3*6)+(2*1)+(1*4)=140
140 % 10 = 0
So 62686-14-0 is a valid CAS Registry Number.
62686-14-0Relevant articles and documents
One-pot synthesis of quinoxalines from reductive coupling of 2-nitroanilines and 1,2-diketones using indium
Go, Ahra,Lee, Geunsoo,Kim, Jaeho,Bae, Seolhee,Lee, Byung Min,Kim, Byeong Hyo
, p. 1215 - 1226 (2015/03/04)
The one-pot reduction-cyclization of 2-nitroanilines and 1,2-diketones to give quinoxalines was investigated. Using indium and an appropriate acid such as acetic acid or indium(III) chloride, various quinoxaline derivatives including 2,3-dialkylquinoxalines, 2,3-diphenylquinoxalines, 2,3-di-2-thiophenylquinoxalines, 2,3-di(pyridin-2-yl)quinoxalines, and dibenzo[a,c]phenazines were synthesized in moderate to excellent yield.
Quinoxaline derivatives as immune regulants
-
, (2008/06/13)
Novel quinoxaline derivatives, useful as immune regulatory agents capable of altering the immune response in mammals.
