118354-71-5 Usage
Description
(S)-1-Benzyl-3-mesyloxy pyrrolidine, with the molecular formula C13H17NO2S, is a chemical compound featuring a pyrrolidine ring structure. This structure is adorned with a benzyl group and a mesyloxy group, the latter being a functional group that includes a sulfonyl group attached to an oxygen atom. The (S) configuration denotes a specific stereoisomeric arrangement, which significantly influences the compound's properties and reactivity in chemical reactions. Given its unique structural attributes and reactivity, (S)-1-Benzyl-3-mesyloxy pyrrolidine holds promise for the development of novel pharmaceuticals and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
(S)-1-Benzyl-3-mesyloxy pyrrolidine is utilized as a reagent in organic synthesis, specifically for the preparation of a variety of pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the creation of new drugs and other biologically active molecules, contributing to advancements in medicinal chemistry and therapeutics.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-1-Benzyl-3-mesyloxy pyrrolidine serves as a key intermediate for the development of complex molecular structures. Its specific stereoisomeric configuration allows for precise control over the outcome of chemical reactions, facilitating the synthesis of target compounds with high selectivity and efficiency.
Used in Drug Development:
The potential applications of (S)-1-Benzyl-3-mesyloxy pyrrolidine extend to the realm of drug development. Its unique structural features and reactivity make it a promising candidate for the design and synthesis of novel therapeutic agents, potentially leading to the discovery of new treatments for various diseases and medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 118354-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118354-71:
(8*1)+(7*1)+(6*8)+(5*3)+(4*5)+(3*4)+(2*7)+(1*1)=125
125 % 10 = 5
So 118354-71-5 is a valid CAS Registry Number.
118354-71-5Relevant articles and documents
Development of a Dual-Acting Antibacterial Agent (TNP-2092) for the Treatment of Persistent Bacterial Infections
Ma, Zhenkun,Lynch, Anthony Simon
, p. 6645 - 6657 (2016/08/05)
The clinical management of prosthetic joint infections and other persistent bacterial infections represents a major unmet medical need. The rifamycins are one of the most potent antibiotic classes against persistent bacterial infections, but bacteria can
METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND
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Page/Page column 18, (2009/05/29)
Aiming at production of an optically active 3-amino nitrogen-containing compound which is useful as an intermediate in synthesis of medicines and pesticides, in particular, an optically active 1-protected-3-aminopyrrolidine derivative, from an inexpensive and readily available raw material by a process which is efficient and can be practiced industrially, an optically active 3-amino nitrogen-containing compound is produced by performing a reaction of an optically active 3-substituted nitrogen-containing compound with ammonia, methylamine, ethylamine or dimethylamine in the presence of water. In addition, a 1-protected-3-aminopyrrolidine derivative is produced by performing a reaction of an optically active 1-protected-3-(sulfonyloxy)pyrrolidine derivative with ammonia, methylamine, ethylamine, or dimethylamine in the presence of methanol, ethanol, n-propanol, or isopropanol under a pressure of less than 30 barr.
Synthesis of beta-proline like derivatives and their evaluation as sodium channel blockers
Muraglia, Marilena,Franchini, Carlo,Corbo, Filomena,Scilimati, Antonio,Sinicropi, Maria Stefania,De Luca, Annamaria,De Bellis, Michela,Camerino, Diana Conte,Tortorella, Vincenzo
, p. 1099 - 1103 (2008/09/17)
(Chemical Equation Presented) A simple and convenient procedure for the preparation of beta-proline like derivatives in their racemic and optically active forms has been reported. The compounds have been screened for their potential activity as sodium cha
