22862-75-5 Usage
Description
(2S,3R,4R)-4-hydroxy-2-(4-methoxybenzyl)pyrrolidin-3-yl acetate hydrochloride (1:1) is a chiral molecule with a pyrrolidin structure, a hydroxyl group, an acetate group, and a methoxybenzyl group, combined with a hydrochloride salt. Its specific stereochemistry (2S,3R,4R) may contribute to its potential pharmaceutical or biological applications, such as serving as a drug or precursor for drug synthesis.
Uses
Used in Pharmaceutical Industry:
(2S,3R,4R)-4-hydroxy-2-(4-methoxybenzyl)pyrrolidin-3-yl acetate hydrochloride (1:1) is used as a potential drug or precursor for drug synthesis due to its unique structure and stereochemistry. The presence of the hydroxyl, acetate, and methoxybenzyl groups, along with the hydrochloride salt, may contribute to its medicinal properties and formulation in pharmaceutical products.
Used in Research Applications:
(2S,3R,4R)-4-hydroxy-2-(4-methoxybenzyl)pyrrolidin-3-yl acetate hydrochloride (1:1) may be utilized in research settings for studying its potential biological activities and interactions with biological targets. The hydrochloride salt form of the compound could be particularly useful in experiments involving the compound's solubility and reactivity in various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22862-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22862-75:
(7*2)+(6*2)+(5*8)+(4*6)+(3*2)+(2*7)+(1*5)=115
115 % 10 = 5
So 22862-75-5 is a valid CAS Registry Number.
22862-75-5Relevant articles and documents
Stereoselective Total Synthesis of Unnatural (+)-Anisomycin
Ajay, Sama,Saidhareddy, Puli,Shaw, Arun K.
, p. 1191 - 1196 (2016/05/11)
Stereoselective total synthesis of unnatural (+)-anisomycin from d-glucose has been achieved with an overall yield of 23%. The key synthetic features are regioselective opening of an epoxide, azidation of the resulting alcohol, and finally one-pot hydroge
An aldol-based approach to the synthesis of the antibiotic anisomycin
Hulme, Alison N.,Rosser, Edward M.
, p. 265 - 267 (2007/10/03)
Chemical equation presented A new approach to the synthesis of the antibiotic anisomycin is reported that relies upon a key aldol disconnection. The glycolate aldol coupling proceeds in 75% yield and with >95% diastereoselectivity, which allows the 13-step synthesis to proceed in 35% overall yield.
