247045-28-9 Usage
General Description
5,6-dibromoisoindoline-1,3-dione, also known as NSC 527179, is an organic chemical compound derived from isoindoline, which itself is a heterocyclic compound. 5,6-dibroMoisoindoline-1,3-dione contains two elements of bromine, which is represented by its dibromo prefix. Isoindoline is the parent structure of this compound, with the 1,3-dione suffix indicating the presence of two ketone functional groups at the 1 and 3 positions of the isoindoline ring system. The properties and potential uses of this specific compound might vary; however, derivatives of isoindoline have found relevance in medicinal chemistry as some exhibit antitumor, anti-inflammatory, or even antidepressant activities.
Check Digit Verification of cas no
The CAS Registry Mumber 247045-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,0,4 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 247045-28:
(8*2)+(7*4)+(6*7)+(5*0)+(4*4)+(3*5)+(2*2)+(1*8)=129
129 % 10 = 9
So 247045-28-9 is a valid CAS Registry Number.
247045-28-9Relevant articles and documents
4,5-Dibromo-phthalimide forms two centrosymmetric dimers, one linked by C - H...O hydrogen bonds and one by N - H...O hydrogen bonds
Williamson, Craig,Harrison, William T. A.
, (2007)
In the title compound [also called 5,6-dibromo-isoindole-1,3(2H)-dione], C8H3Br2NO2, there are two planar mol-ecules in the asymmetric unit. They both form inversion dimers, one via N - H...O links and one via short near-linear C - H...O links. The dimers
Synthesis of ladder-type oligomers incorporating phthalocyanine units
Hanack, Michael,Stihler, Patrick
, p. 303 - 311 (2007/10/03)
The condensation of substituted diiminoisoindolines with alkyl- substituted 1,3,3-trichloroisoindolines results in the formation of the highly soluble metal-free phthalocyanines 9, 15. By the same methodology, metal-containing phthalocyanines such as 16,
