210468-90-9 Usage
Uses
Used in Pharmaceutical Research:
(4S,5S)-1,3-DIMETHYL-4,5-DIPHENYL-2-[(R)-1-BENZYL-2-HYDROXYETHYLIMINO]IMIDAZOLIDINE is used as a research compound for exploring its potential biological activities and interactions with various molecular targets. Its unique structure and stereochemistry may contribute to its efficacy in modulating specific biological pathways or as a lead compound in drug discovery processes.
Used in Organic Synthesis:
As a building block in organic synthesis, (4S,5S)-1,3-DIMETHYL-4,5-DIPHENYL-2-[(R)-1-BENZYL-2-HYDROXYETHYLIMINO]IMIDAZOLIDINE can be utilized for the creation of more complex molecules with specific functions or properties. Its versatile structure allows for further chemical modifications, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Chiral Chemistry:
Due to its chiral centers, (4S,5S)-1,3-DIMETHYL-4,5-DIPHENYL-2-[(R)-1-BENZYL-2-HYDROXYETHYLIMINO]IMIDAZOLIDINE is used in chiral chemistry to study the effects of stereochemistry on biological activity, reactivity, or selectivity. (4S,5S)-1,3-DIMETHYL-4,5-DIPHENYL-2-[(R)-1-BENZYL-2-HYDROXYETHYLIMINO]IMIDAZOLIDINE can also be employed as a chiral auxiliary or ligand in asymmetric synthesis to induce enantioselectivity in chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 210468-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,4,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 210468-90:
(8*2)+(7*1)+(6*0)+(5*4)+(4*6)+(3*8)+(2*9)+(1*0)=109
109 % 10 = 9
So 210468-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H29N3O/c1-28-24(21-14-8-4-9-15-21)25(22-16-10-5-11-17-22)29(2)26(28)27-23(19-30)18-20-12-6-3-7-13-20/h3-17,23-25,30H,18-19H2,1-2H3/t23-,24+,25+/m1/s1
210468-90-9Relevant academic research and scientific papers
Isobe,Fukuda,Ishikawa
, p. 7770 - 7773 (2000)
Modified guanidines were explored as potential chiral superbases. Thus, chiral 1,3-dimethyl-2-iminoimidazolidines with or without 4,5-diphenyl groups, their guanidinium salts, and the 2-iminoimidazolidines with (S)-1-phenylethyl groups on the ring nitrogens were prepared by treatment of 2-chloroimidazolinium chlorides with appropriate amines. Bicyclic guanidines were also prepared from a prolinamide using a similar procedure.
