67651-47-2 Usage
Azepine family
1H-Azepine-1-carboxamide, hexahydro-(9CI) belongs to the azepine family of chemical compounds.
Saturated cyclic organic compound
It is a saturated cyclic organic compound with a six-membered ring.
Nitrogen atom
The six-membered ring contains a nitrogen atom.
Carboxamide functional group
The compound has a carboxamide functional group.
Synonym
It is also known as capracanone A.
Pharmaceutical industry use
It is primarily used in the pharmaceutical industry as a building block for the synthesis of various drugs and active pharmaceutical ingredients.
Potential applications in drug discovery
Due to its unique structural properties and biological activities, it has potential applications in drug discovery and development.
Organic synthesis and chemical research applications
It may also have applications in the field of organic synthesis and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 67651-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67651-47:
(7*6)+(6*7)+(5*6)+(4*5)+(3*1)+(2*4)+(1*7)=152
152 % 10 = 2
So 67651-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O/c8-7(10)9-5-3-1-2-4-6-9/h1-6H2,(H2,8,10)
67651-47-2Relevant articles and documents
Regioselective Formal [3+2] Cycloadditions of Urea Substrates with Activated and Unactivated Olefins for Intermolecular Olefin Aminooxygenation
Wu, Fan,Alom, Nur-E,Ariyarathna, Jeewani P.,Na?, Johannes,Li, Wei
supporting information, p. 11676 - 11680 (2019/07/31)
A new class of intermolecular olefin aminooxygenation reaction is described. This reaction utilizes the classic halonium intermediate as a regio- and stereochemical template to accomplish the selective oxyamination of both activated and unactivated alkenes. Notably, urea chemical feedstock can be directly introduced as the N and O source and a simple iodide salt can be utilized as the catalyst. This formal [3+2] cycloaddition process provides a highly modular entry to a range of useful heterocyclic products with excellent selectivity and functional-group tolerance.
