229978-45-4 Usage
Uses
Used in Pharmaceutical Industry:
(2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole is used as a potential pharmaceutical agent for its unique chemical structure and properties. (2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole's specific stereochemistry and aromatic nature may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole serves as a subject of study for understanding the properties and reactivity of imidazo[1,2-a]imidazoles. Its complex ring structure and stereochemistry make it an interesting compound for exploring the effects of molecular geometry on chemical behavior.
Used in Material Science:
(2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole may also find applications in material science, where its unique structure and properties could be leveraged to develop new materials with specific characteristics. (2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole's aromatic nature and stereochemistry could influence its electronic, optical, or mechanical properties, making it a candidate for use in advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 229978-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,9,7 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 229978-45:
(8*2)+(7*2)+(6*9)+(5*9)+(4*7)+(3*8)+(2*4)+(1*5)=194
194 % 10 = 4
So 229978-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H17N3/c1-3-7-13(8-4-1)15-11-20-12-16(19-17(20)18-15)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,18,19)/t15-,16-/m0/s1
229978-45-4Relevant academic research and scientific papers
Enantioselective synthesis of α-amino nitriles from N-benzhydryl imines and HCN with a chiral bicyclic guanidine as catalyst
Corey,Grogan, Michael J.
, p. 157 - 160 (2008/03/11)
(Equation Presented) A novel catalytic enantioselective Strecker synthesis of chiral α-amino nitriles and α-amino acids is described and analyzed with regard to the possible mechanistic basis for stereoselectivity. Key features of the enantioselective process include (1) the use of the chiral bicyclic guanidine 1 as catalyst and (2) the use of the N-benzhydryl substituent on the imine substrate.
