293732-31-7 Usage
Molecular structure
1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodo-4,5-dimethoxyphenyl)methyl]contains a pyrrole ring, a carboxamide group, diethyl and methyl substituents, an iodine atom, and two methoxy groups attached to a phenyl moiety.
Synthetic compound
1H-Pyrrole-2-carboxamide,
N,N-diethyl-1-[(2-iodo-4,5-dimethoxyphenyl)methyl]- is a synthetic chemical substance, which means it is man-made and not found naturally in the environment.
Pharmaceutical applications
The compound has potential pharmaceutical applications, which means it could be used in the development of drugs or in medicinal chemistry research.
Biological activity
The presence of specific structural elements in the compound suggests that it may have biological activity, which means it could interact with biological systems and potentially produce therapeutic effects.
Further research needed
Additional studies are required to fully understand the potential uses and properties of 1H-Pyrrole-2-carboxamide,
N,N-diethyl-1-[(2-iodo-4,5-dimethoxyphenyl)methyl]-, as its effects on biological systems and potential applications are not yet fully known.
Check Digit Verification of cas no
The CAS Registry Mumber 293732-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,7,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 293732-31:
(8*2)+(7*9)+(6*3)+(5*7)+(4*3)+(3*2)+(2*3)+(1*1)=157
157 % 10 = 7
So 293732-31-7 is a valid CAS Registry Number.
293732-31-7Relevant academic research and scientific papers
Synthesis of pyrrolo[1,2-b]isoquinolines through mesityllithium-mediated intramolecular carbolithiation
Lage, Sergio,Villaluenga, Irune,Sotomayor, Nuria,Lete, Esther
experimental part, p. 3188 - 3192 (2009/06/18)
Mesityllithium has proven to be an effective iodine-lithium exchange reagent. Thus, carbolithiation reactions on 2-alkenyl-substituted N-(o-iodobenzyl)pyrroles have been accomplished avoiding side reactions to afford pyrroloisoquinolines in high yields (8
An efficient entry to pyrrolo[1,2-b]isoquinolines and related systems through Parham cyclisation
Ruiz, Javier,Ardeo, Ainhoa,Ignacio, Roberto,Sotomayor, Nuria,Lete, Esther
, p. 3311 - 3324 (2007/10/03)
Aryllithiums generated by lithium-iodine exchange undergo intramolecular cyclisation to give pyrrolo[1,2-b]isoquinolines, in high yields. The best results were obtained when Weinreb or morpholine amides were used as internal electrophiles. The procedure h
Metalation-cyclisation sequence on N-(o-halobenzyl)pyrroles. Synthesis of pyrrolo[1,2-b]isoquinolones
Ardeo, Ainhoa,Lete, Esther,Sotomayor, Nuria
, p. 5211 - 5214 (2007/10/03)
Parham-type cyclisation of N-(o-halobenzyl)pyrroles has been investigated. Aryllithiums generated from metalation of N-(o- iodobenzyl)pyrroles undergo intramolecular cyclisation to give pyrrolo[1,2- b]isoquinolinones in moderate to good yields, if the N,N
