88710-42-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 8 hydrogen (H) atoms, and 2 nitrogen (N) atoms.
Explanation
The compound consists of two fused heterocyclic rings, an imidazole and a pyrazine, with a phenyl group (C6H5) attached to the 2nd position of the imidazo[4,5-b]pyrazine ring.
Explanation
The compound is classified as an aromatic compound due to the presence of the imidazole and pyrazine rings, which are known for their aromatic properties.
Explanation
The compound has been studied for its potential pharmacological properties, which may lead to its use in the development of new drugs and pharmaceuticals.
Explanation
Due to its unique structure, 1H-Imidazo[4,5-b]pyrazine, 2-phenylcan be used as a starting material or building block in the synthesis of various other organic compounds.
Explanation
The compound's structure and properties make it an interesting molecule for researchers to explore its potential in the development of new drugs and pharmaceuticals.
Explanation
The material provided does not give information about the chemical stability of the compound. Further research would be needed to determine its stability under various conditions.
Explanation
The material provided does not mention the solubility of the compound in different solvents. Solubility is an important property for determining the compound's suitability in various applications.
Explanation
The material provided does not provide information about the reactivity of the compound with other chemicals. Reactivity is a crucial factor in determining the compound's potential use in medicinal chemistry and other applications.
Explanation
The material provided does not discuss the toxicity of the compound. Toxicity is an essential factor to consider when evaluating the compound's potential use in pharmaceuticals and other applications.
Structure
Imidazole and pyrazine ring system with a phenyl group at position 2
Aromaticity
Heterocyclic aromatic compound
Pharmacological Properties
Potential use in medicinal chemistry
Application
Building block in the synthesis of other organic compounds
Research Interest
Development of new drugs and pharmaceuticals
Chemical Stability
Unknown
Solubility
Unknown
Reactivity
Unknown
Toxicity
Unknown
Check Digit Verification of cas no
The CAS Registry Mumber 88710-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88710-42:
(7*8)+(6*8)+(5*7)+(4*1)+(3*0)+(2*4)+(1*2)=153
153 % 10 = 3
So 88710-42-3 is a valid CAS Registry Number.
88710-42-3Relevant articles and documents
A facile access for the synthesis of some C-2 substituted imidazopyrazines by utilizing the palladium catalyzed Suzuki cross-coupling reaction under microwave irradiation
Joy, M. Nibin,Savitha, Bhaskaran,Sajith, Ayyiliyath M.,Bodke, Yadav D.,Venkatesh, Talavara,Khader, K.K. Abdul,Padusha, M. Syed Ali,Muralidharan
, p. 31 - 36 (2016)
A rapid, efficient, and facile synthesis of an assortment of C-2 substituted imidazopyrazines has been achieved by utilizing the palladium catalyzed Suzuki cross-coupling of 2-bromo-1H-imidazo[4,5-b]pyrazine with various boronic acids under microwave irradiation. The utilization of (A-taphos)2PdCl2 as a catalyst in combination with CsF as base and DME-H2O (4:1) as the solvent system at 100°C procured the diaryls in acceptable to excellent yields. Prominent features of this developed methodology include short reaction times, fewer side products, and exceptional tolerance to a wide variety of functional groups.
