3623-90-3 Usage
Uses
As the provided materials do not specify any particular applications for 2-[4-(1,3-dioxoisoindol-2-yl)butyl]isoindole-1,3-dione, it is not possible to list specific uses or industries for 2-[4-(1,3-dioxoisoindol-2-yl)butyl]isoindole-1,3-dione based on the information given. However, given its complex structure and potential pharmaceutical relevance, it could be hypothesized that 2-[4-(1,3-dioxoisoindol-2-yl)butyl]isoindole-1,3-dione might be used in the following ways:
Used in Pharmaceutical Industry:
2-[4-(1,3-dioxoisoindol-2-yl)butyl]isoindole-1,3-dione could be utilized as a pharmaceutical agent for [specific medical condition or treatment] due to its unique structure and potential to interact with biological systems.
Used in Chemical Research:
In the field of chemical research, 2-[4-(1,3-dioxoisoindol-2-yl)butyl]isoindole-1,3-dione might serve as a subject for studying [specific chemical interactions or reactions] because of its distinctive functional groups and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 3623-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,2 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3623-90:
(6*3)+(5*6)+(4*2)+(3*3)+(2*9)+(1*0)=83
83 % 10 = 3
So 3623-90-3 is a valid CAS Registry Number.
3623-90-3Relevant academic research and scientific papers
Thalidomide analogs from diamines: Synthesis and evaluation as inhibitors of TNF-α production
De Almeida, Mauro Vieira,Teixeira, Francisco Martins,De Souza, Marcus Vinicius Nora,Amarante, Giovanni Wilson,Alves, Caio Cesar De Souza,Cardoso, Silvia Helena,Mattos, Ana Marcia,Ferreira, Ana Paula,Teixeira, Henrique Couto
, p. 223 - 226 (2007/10/03)
Fourteen thalidomide analogs bearing two phthalimido units were prepared in high yields (83-94%) by condensation of different diamines with phthalic or 3-nitrophthalic anhydride. An in vitro investigation of the compounds as inhibitors of the TNF-α production was performed. The inhibition was higher for compounds bearing amino and nitro groups and was modulated by increasing the size of the spacers between the phthalimide groups.
Modified procedure for preparing δ-[2,4-di(tert-amyl)phenoxy]butylamine
Yutilov,Svertilova,Minkina,Shcherbina,Kirillova
, p. 2106 - 2108 (2007/10/03)
A modified procedure is proposed for preparing δ-[2,4-di(tert-amyl)phenoxy]butylamine used in production of a blue protected component for color photographic materials.
