126070-15-3 Usage
General Description
The chemical "2-(3,4-dichlorophenyl)isoquinoline-1,3(2H,4H)-dione" is a complex organic compound with a unique molecular structure. It contains a isoquinoline-1,3-dione core with two chlorine atoms attached to the phenyl group at positions 3 and 4. This chemical may have potential applications in medicinal chemistry and drug development due to its structural properties. It is likely to have biological activity and may be used as a building block for the synthesis of new pharmaceutical compounds. The presence of the isoquinoline-1,3-dione scaffold suggests that it could exhibit various pharmacological activities, making it an attractive target for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 126070-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126070-15:
(8*1)+(7*2)+(6*6)+(5*0)+(4*7)+(3*0)+(2*1)+(1*5)=93
93 % 10 = 3
So 126070-15-3 is a valid CAS Registry Number.
126070-15-3Relevant articles and documents
2-BENZENEACETIC ACIDS AFFECTING ROOT GRAVITROPISM
Modena, T.,Azzolina, O.,Genta, I.,Mazza, M.
, p. 721 - 730 (2007/10/02)
A series of new 2-benzeneacetic acids , prepared by basic hydrolysis of 2-substituted 1,3(2H-4H)isoquinolinediones, were studied from the point of view of their antigravitropic activity on germinating seeds of Lens esculenta Moench.The results of the assay showed that the class possesses antigravitropic activity.The most active compounds were the dichlorosubstituted phenyl-derivatives (XXI), (XVII) and (XX), 2-naphthyl- (XXIV), 8-quinolyl- (XXV) and 4-biphenylyl- (IX) derivatives.The activity of the class is generally lower than that of the the homologous N-arylphthalamic acids.Moreover the trifluoromethyl-phenyl- (III) and the 1-naphthyl- (XXIII) derivatives, subjected to herbicidal assay against some common weeds, showed a noticeable activity, with marked selectivity against Dicotyledons.