96562-96-8 Usage
Description
2-BROMO-6,7-DIHYDRO-1H,5H-PYRROLO[2,3-C]AZEPINE-4,8-DIONE is a complex chemical compound characterized by a pyrroloazepine backbone, which includes a pyrrole and a 7-membered ring. 2-BROMO-6,7-DIHYDRO-1H,5H-PYRROLO[2,3-C]AZEPINE-4,8-DIONE features a 1H,5H-pyrrolo[2,3-c]azepine-4,8-dione core, indicating the presence of a pyrroloazepine ring system with a dione functional group at positions 4 and 8. The inclusion of a bromine atom further contributes to its unique molecular structure, suggesting potential for various pharmacological and medicinal applications. It may serve as a building block for the synthesis of biologically active molecules or as a candidate for drug development.
Uses
Used in Pharmaceutical Industry:
2-BROMO-6,7-DIHYDRO-1H,5H-PYRROLO[2,3-C]AZEPINE-4,8-DIONE is used as a chemical intermediate for the synthesis of biologically active molecules. Its unique structure, including the pyrroloazepine backbone and the dione functional group, makes it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-BROMO-6,7-DIHYDRO-1H,5H-PYRROLO[2,3-C]AZEPINE-4,8-DIONE is utilized as a starting point for designing and optimizing novel compounds with specific pharmacological properties. Its structural features can be modified to explore various avenues in drug discovery, potentially leading to the creation of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 96562-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96562-96:
(7*9)+(6*6)+(5*5)+(4*6)+(3*2)+(2*9)+(1*6)=178
178 % 10 = 8
So 96562-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrN2O2/c9-6-3-4-5(12)1-2-10-8(13)7(4)11-6/h3,11H,1-2H2,(H,10,13)
96562-96-8Relevant articles and documents
Acid catalyzed halogen dance on deactivated pyrroles
Tutino, Federico,Papeo, Gianluca,Quartieri, Francesca
supporting information; experimental part, p. 112 - 117 (2010/04/23)
(Chemical Equation Presented) A study on the acid catalyzed halogen dance (ACHD) on deactivated bromopyrroles is reported. A different behavior is observed when considering singly deactivated pyrrole alkylcarboxamides, or doubly deactivated pyrroleketo-lactams (aldisines). Although less electron deficient pyrrole alkylcarboxamides suffer from ACHD, the double deactivation on keto-lactams disfavors pyrrole ring protonation thus preventing halogen scrambling. The mechanism involved in the rearrangement is hypothesized.
Total Syntheses of Hymenialdisine and Debromohymenialdisine: Stereospecific Construction of the 2-Amino-4-Oxo-2-Imidazolin-5(Z)-Disubstituted Ylidene Ring System
Annoura, Hirokazu,Tatsuoka, Toshio
, p. 413 - 416 (2007/10/02)
The first total synthesis of hymenialdisine (1a) and debromohymenialdisine (1b) was achieved via a novel stereospecific construction of the 2-amino-4-oxo-2-imidazoline-5(Z)-disubstituted ylidine ring system.
