87708-01-8 Usage
Description
(2S,3R,10R,10aS)-10,10a-dimethyl-1,2,3,4,10,10a-hexahydro-2,10-epithiopyrimido[1,2-a]indole-3-carbonitrile is a complex organic molecule with a hexahydroindole core and a carbonitrile functional group. It is a chiral compound with two stereocenters, designated as 2S,3R and 10R,10aS. (2S,3R,10R,10aS)-10,10a-dimethyl-1,2,3,4,10,10a-hexahydro-2,10-epithiopyrimido[1,2-a]indole-3-carbonitrile has a dimethyl group at the 10 and 10a positions, and an epithio ring fusion between the 2 and 10 positions. This molecule may have potential applications in medicinal chemistry, as it possesses a unique and intricate structure that could be relevant for drug design or other research purposes.
Uses
Used in Medicinal Chemistry:
(2S,3R,10R,10aS)-10,10a-dimethyl-1,2,3,4,10,10a-hexahydro-2,10-epithiopyrimido[1,2-a]indole-3-carbonitrile is used as a potential candidate for drug design due to its unique and intricate structure. Its chiral centers and specific functional groups may allow for targeted interactions with biological targets, making it a promising compound for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 87708-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,0 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87708-01:
(7*8)+(6*7)+(5*7)+(4*0)+(3*8)+(2*0)+(1*1)=158
158 % 10 = 8
So 87708-01-8 is a valid CAS Registry Number.
87708-01-8Relevant articles and documents
1,3-DIPOLAR CYCLOADDITION OF THIAZOLIUM N-PHENYLIMIDES WITH ACRYLONITRILE
Hirano, Hiroshi,Sugiyama, Kazuaki,Yamashita, Mayumi,Inoue, Masatoshi,Ishida, Toshimasa
, p. 1792 - 1795 (2007/10/02)
3-Anilinothiazolium salt(1) was synthesized via three steps from ammonium 3-phenyldithiocarbazate, and the cycloaddition reaction of the ylide(2) prepared from 1 with acrylonitrile was carried out in two different solvents, DMF and methanol.The reaction in DMF produced two compounds, derivatives of 2,3,3a,8b-tetrahydro-4H-2,4-ethanothiazoloindole (3a and 3b), while the similar reaction in methanol unexpectedly gave bis(4,5-dimethyl-2-thiazolyl)cyanomethane (5).The structures of 3a and 3b were established by the 1H-NMR (400 MHz) spectral data and the X-ray analysis.KEYWORDS - 1,3-dipolar cycloaddition; thiazolium N-phenylimide; 2,3,3a,8b-tetrahydro-4H-2,4-ethanothiazoloindole; 1H-NMR (400 MHz); X-ray analysis; sigmatropic rearrangement; bis(4,5-dimethyl-2-thiazolyl)cyanomethane
