205648-91-5 Usage
Chemical structure
A complex, multi-ring structure containing a hexahydro-1H-isoquinoline group with a 4-methoxy-benzyl substituent and an ethanone group.
Chirality
The "R" configuration indicates that the compound is chiral, meaning it has a specific three-dimensional arrangement of atoms that is not superimposable on its mirror image.
Pharmacological or biological activities
The compound may have potential pharmacological or biological activities due to its complex structure, which could allow it to interact with biological targets or participate in chemical reactions.
Further research and experimentation
The exact properties and uses of 1-[(R)-1-(4-Methoxy-benzyl)-3,4,5,6,7,8-hexahydro-1H-isoquinolin-2-yl]-ethanone would need to be determined through additional research and experimentation, as its potential applications and effects are not yet fully understood.
Molecular weight
Approximately 311.4 g/mol (calculated from the molecular formula)
Functional groups
The compound contains an isoquinoline ring, a benzyl group with a methoxy substituent, and a ketone group.
Stability
The stability of the compound under various conditions (e.g., temperature, pH, etc.) would need to be determined through further research.
Synthesis
The synthesis of 1-[(R)-1-(4-Methoxy-benzyl)-3,4,5,6,7,8-hexahydro-1H-isoquinolin-2-yl]-ethanone would likely involve multiple steps, including the formation of the isoquinoline ring, the introduction of the 4-methoxy-benzyl group, and the attachment of the ethanone group.
Check Digit Verification of cas no
The CAS Registry Mumber 205648-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,6,4 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 205648-91:
(8*2)+(7*0)+(6*5)+(5*6)+(4*4)+(3*8)+(2*9)+(1*1)=135
135 % 10 = 5
So 205648-91-5 is a valid CAS Registry Number.
205648-91-5Relevant academic research and scientific papers
Heiser,Broger,Crameri
, p. 51 - 62 (1991)
A new synthetically useful method for the synthesis of the diphosphine ruthenium dicarboxylato complexes (P-P)Ru(O2CR)2(R= CF3 and CH3) is presented, which uses the easily accessible complex (COD)2Ru2(μ-O2CCF3)4 as starting material. This complex as well as (COD)(Ru(ηO2CCH3)2 and (COD)2Ru2Cl4(NCCH3) have been shown to be suitable precursor complexes for the in-situ preparation of ruthenium(II) dicarboxylato and dichloro complexes of atropisomeric diphosphines, respectively. The high efficacy of the preformed and in-situ generated ruthenium complexes as precatalysts is demonstrated in asymmetric hydrogenations of allylic alcohols, enamides, and a β-keto ester.
