91658-36-5 Usage
Description
(S)-2-METHOXYMETHYL-1-METHYLIDENEAMINO-PYRROLIDINE is a chiral chemical compound derived from the pyrrolidine structure, featuring a methylideneamino group and a methoxymethyl group attached to the second carbon atom. As a chiral molecule, it possesses a non-superimposable mirror image and exists as a pair of enantiomers. Its unique structure may endow it with potential biological activity, making it a candidate for pharmaceutical development. However, further research and testing are required to ascertain its specific properties and potential applications.
Uses
Used in Pharmaceutical Development:
(S)-2-METHOXYMETHYL-1-METHYLIDENEAMINO-PYRROLIDINE is used as a potential building block for the development of new pharmaceuticals due to its unique structure and possible biological activity. Its chiral nature may offer advantages in targeting specific biological pathways or receptors, which could be beneficial in creating more effective and selective medications.
Used in Research and Development:
In the field of chemical research, (S)-2-METHOXYMETHYL-1-METHYLIDENEAMINO-PYRROLIDINE serves as a valuable compound for studying the effects of chirality on biological activity and understanding the interactions between molecules and their targets. This knowledge can be applied to the design of more effective drugs and the optimization of existing pharmaceuticals.
Used in Drug Synthesis:
(S)-2-METHOXYMETHYL-1-METHYLIDENEAMINO-PYRROLIDINE may be utilized as an intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting specific receptors or biological pathways. Its unique structure could provide a foundation for the development of novel drugs with improved efficacy and selectivity.
Used in Chiral Catalysts:
The chiral nature of (S)-2-METHOXYMETHYL-1-METHYLIDENEAMINO-PYRROLIDINE may also make it a candidate for use in the development of chiral catalysts, which are essential in various chemical reactions, particularly in the synthesis of enantiomerically pure compounds. These catalysts can improve the efficiency and selectivity of chemical processes, leading to more sustainable and cost-effective production methods in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 91658-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91658-36:
(7*9)+(6*1)+(5*6)+(4*5)+(3*8)+(2*3)+(1*6)=155
155 % 10 = 5
So 91658-36-5 is a valid CAS Registry Number.
91658-36-5Relevant articles and documents
ARGININE METHYLTRANSFERASE INHIBITORS AND USES THEREOF
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Paragraph 00394, (2014/10/04)
Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds described herein are useful for inhibiting arginine methyltransferase activity. Methods of using the compounds for treating arginine methyltransferase-mediated disorders are also described.
ASYMMETRIC SYNTHESES VIA METALATED CHIRAL HYDRAZONESOVERALL ENANTIOSELECTIVE α-ALKYLATION OF ACYCLIC KETONES
Enders, D.,Eichenauer, H.,Baus, U.,Schubert, H.,Kremer, K. A. M.
, p. 1345 - 1359 (2007/10/02)
A general method is described, which allows the overall enantioselective α-alkylation of acyclic ketones in good overall yields (44-86percent, 4 steps) and enantioselectivities ranging routinely from >94percent ee up to virtually complete asymmetric induction (99.5percent ee).The acyclic ketones are transformed to their corresponding "SAMP-hydrazones" (S)-2 by reaction with the enantiomerically pure hydrazine (S)-1-amino-2-methoxymethyl-pyrrolidine , readily available from (S)-proline.Metalation to form chiral azaenolates (S)-3 of ECCZCN-configuration and then alkylation to product hydrazones 4, followed by hydrazone cleavage via acidic hydrolysis of methiodides 9 in a two phase system or ozonolysis, leads to α-substituted, enantiomerically enriched, acyclic ketones 5.In special cases, where a phenyl group is directly attached to the newly generated center of chirality (5n,o,p), only low enantiomeric excesses are observed. 17 Examples, including first applications in natural product synthesis (cf 5a,b,e, and h) are summarized.
