102976-63-6 Usage
Structure
A heterocyclic aromatic compound with a benzene ring and an imidazole ring fused together, with a hydroxyl group at the 2-position and a methyl group at the 1-position.
Properties
The presence of the methyl group at the 1-position of the benzimidazole ring gives this compound its specific properties and reactivity.
Uses
It may be used in various organic synthesis processes and as a building block for the preparation of other compounds.
Biological activities
It is of interest for its potential biological activities and could be studied as a potential drug candidate.
Note
Its specific uses and properties may vary depending on the context of its application and further research may be necessary to fully understand its potential uses and hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 102976-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,7 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102976-63:
(8*1)+(7*0)+(6*2)+(5*9)+(4*7)+(3*6)+(2*6)+(1*3)=126
126 % 10 = 6
So 102976-63-6 is a valid CAS Registry Number.
102976-63-6Relevant articles and documents
Highly stereoselective formal synthesis of rosuvastatin and pitavastatin through Julia-Kocienski olefination using the lactonized statin side-chain precursor
Fabris, Jan,?asar, Zdenko,Smilovi?, Ivana Gazi?,?rnugelj, Martin
, p. 2333 - 2346 (2014/12/09)
An expedient and simple synthetic approach to pitava statin and rosuvastatin final intermediates is described. The presented approach consists of completely stereoselective Julia-Kocienski olefination step (E/Z up to 300:1) between lactonized statin side-chain precursor and sulfone derivative of the corresponding pyrimidine and quinoline heterocyclic cores. The desired O-TBS protected statin lactones were isolated in 66-71% yield and high >97% purity (HPLC). Georg Thieme Verlag Stuttgart. New York.
STEREOSELECTIVE SYNTHESIS OF D- AND L-RIBOSE
Yamaguchi, Masahiko,Mukaiyama, Teruaki
, p. 1005 - 1008 (2007/10/02)
The allylcadmiun compound, prepared in situ from 2-allyl-oxybenzimidazole, reacts with 2,4-O-isopropylidene-D and L-glyceraldehyde in highly regio- and stereoselective manner to give the corresponding enantiomeric adducts.The adducts are further transform
