351996-94-6 Usage
Chemical Class
The compound belongs to the class of isoindoline-1,3-dione derivatives.
Appearance
It is a white solid.
Solubility
The compound is soluble in organic solvents such as methanol and chloroform.
Pharmaceutical Applications
2-(4-Methoxybenzyl)-1,3-dioxoisoindoline-5-carboxylic acid has potential pharmaceutical applications due to its biological activities.
Biological Activities
The compound has anti-inflammatory and cytotoxic properties.
Structure-Activity Relationship
The presence of the methoxybenzyl group and carboxylic acid functionality in its structure contributes to its pharmacological activity.
Chemical Structure
It is a derivative of isoindoline-1,3-dione, which is a common motif in many biologically active compounds.
Research and Development
2-(4-Methoxybenzyl)-1,3-dioxoisoindoline-5-carboxylic acid demonstrates potential for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 351996-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,9,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 351996-94:
(8*3)+(7*5)+(6*1)+(5*9)+(4*9)+(3*6)+(2*9)+(1*4)=186
186 % 10 = 6
So 351996-94-6 is a valid CAS Registry Number.
351996-94-6Relevant articles and documents
Design, synthesis, and biological evaluation of 1,3-dioxoisoindoline-5-carboxamide derivatives as T-type calcium channel blockers
Kim, Hwa Sil,Kim, Yoonjee,Doddareddy, Munikumar Reddy,Seo, Seon Hee,Rhim, Hyewhon,Tae, Jinsung,Pae, Ae Nim,Choo, Hyunah,Cho, Yong Seo
, p. 476 - 481 (2007/10/03)
A small molecule library of 1,3-dioxoisoindoline-5-carboxamides 4 was designed based on the pharmacophore model, synthesized and biologically evaluated as potential T-type calcium channel blockers. The most active compounds 4d and 4n show T-type calcium c
