229978-45-4 Usage
General Description
"(2R,6R)-2,3,5,6-Tetrahydro-2,6-diphenyl-1H-imidazo[1,2-a]imidazole" is a chemical compound with a complex ring structure, hinted at by the multiple indexes within its name. It belongs to the class of organic compounds known as imidazo[1,2-a]imidazoles, which are polycyclic aromatic compounds containing an imidazole ring fused to an imidazole ring. It is characterized by its 2,6-diphenyl moiety and the 2R,6R descriptors indicate the compound's stereochemical configuration, indicating the orientation of atoms in the molecule. Specific properties such as its physical state, reactivity, and applications depend on the specific context it is used in.
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 articles and documents
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.
