126070-11-9 Usage
Derivative of isoquinoline
A heterocyclic compound commonly found in various natural products and pharmaceuticals, with a similar structure to isoquinoline but with modifications in its chemical structure.
Chlorine atom and methyl group attached to the phenyl ring
The presence of a chlorine atom and a methyl group (CH3) on the phenyl ring contributes to the compound's unique chemical properties and reactivity.
Carbonyl group on the isoquinoline ring
A carbonyl group (C=O) is present on the isoquinoline ring, which influences the compound's reactivity and potential applications.
Potential applications in pharmaceutical and chemical industries
Due to its unique structural features and properties, this compound may have potential uses in the development of new drugs or chemical processes.
Need for additional research and studies
Further investigation is required to fully understand the compound's potential uses, effects, and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 126070-11-9 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 126070-11:
(8*1)+(7*2)+(6*6)+(5*0)+(4*7)+(3*0)+(2*1)+(1*1)=89
89 % 10 = 9
So 126070-11-9 is a valid CAS Registry Number.
126070-11-9Relevant 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.
