359882-13-6 Usage
Derivative of pyrrolidine
Yes
It is derived from the pyrrolidine structure, which is a five-membered ring containing two nitrogen atoms.
Chiral center
2R designation
The compound has a chiral center, which means it can exist in different spatial arrangements called enantiomers. The "2R" indicates a specific configuration of the chiral center.
Enantiomer
Single enantiomer
The compound exists as a single enantiomer, which means it has a specific spatial arrangement of atoms.
Applications
Pharmaceutical synthesis and organic chemistry research
It is used in the synthesis of pharmaceuticals and other organic compounds, as well as a research tool in organic chemistry.
Potential applications
Development of new drugs
The compound has potential applications in the development of new drugs due to its unique structure and properties.
Structure
2-[(2-bromophenyl)methyl]-4-oxo-, 2-methyl 1-(phenylmethyl) ester
The compound has a complex structure with a bromophenylmethyl group, an oxo group, a methyl group, and a phenylmethyl ester group attached to the pyrrolidine core.
Check Digit Verification of cas no
The CAS Registry Mumber 359882-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,8,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 359882-13:
(8*3)+(7*5)+(6*9)+(5*8)+(4*8)+(3*2)+(2*1)+(1*3)=196
196 % 10 = 6
So 359882-13-6 is a valid CAS Registry Number.
359882-13-6Relevant articles and documents
Synthesis of (-)-aphanorphine using a sulfur-directed aryl radical cyclization
Tamura, Osamu,Yanagimachi, Takehiko,Ishibashi, Hiroyuki
, p. 3033 - 3041 (2007/10/03)
Treatment of radical precursor 15a having a vinyl sulfide moiety with Bu3SnH in the presence of AIBN in boiling benzene afforded exclusively the 6-exo cyclization product 16a, whereas similar treatment of the exo-methylene compound 15b gave a mixture of the 6-exo cyclization product 16b and the endo-olefin product 17 formed by a 1,5-hydrogen shift. Based on these findings, the synthesis of (-)-aphanorphine was achieved using a sulfur-directed 6-exo-selective aryl radical cyclization of 22.
