126070-15-3 Usage
Molecular structure
2-(3,4-dichlorophenyl)isoquinoline-1,3(2H,4H)-dione has a complex organic structure, featuring an isoquinoline-1,3-dione core and a phenyl group with two chlorine atoms attached at positions 3 and 4.
Core structure
The compound contains an isoquinoline-1,3-dione scaffold, which is a common structural motif in many biologically active compounds and can be found in various natural products and pharmaceuticals.
Chlorine substitution
Two chlorine atoms are attached to the phenyl group at positions 3 and 4, which can influence the compound's reactivity, polarity, and lipophilicity, potentially affecting its biological activity and pharmacokinetic properties.
Potential applications
Due to its unique structure and the presence of the isoquinoline-1,3-dione scaffold, this chemical may have potential applications in medicinal chemistry and drug development.
Biological activity
The compound is likely to have biological activity, making it a promising candidate for further research and development in the field of pharmacology and toxicology.
Building block for synthesis
2-(3,4-dichlorophenyl)isoquinoline-1,3(2H,4H)-dione may be used as a building block for the synthesis of new pharmaceutical compounds, potentially leading to the development of novel therapeutic agents.
Attractive target for research
The presence of the isoquinoline-1,3-dione scaffold and the chlorine substitution make this compound an attractive target for further research and development, as it could exhibit various pharmacological activities and properties.
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.
