CAS 74572-13-7
:(S)-2-Methyl-morpholine
Description:
(S)-2-Methyl-morpholine is a chiral organic compound belonging to the morpholine family, characterized by a six-membered ring containing both nitrogen and oxygen atoms. Its molecular structure features a methyl group attached to the second carbon of the morpholine ring, which contributes to its stereochemistry. This compound is typically a colorless to pale yellow liquid with a distinctive amine-like odor. It is soluble in water and various organic solvents, making it versatile in chemical applications. (S)-2-Methyl-morpholine is often utilized as a building block in organic synthesis, particularly in the pharmaceutical industry, due to its ability to act as a nucleophile or a base in reactions. Additionally, its chiral nature allows it to participate in asymmetric synthesis, which is crucial for producing enantiomerically pure compounds. Safety data indicates that it should be handled with care, as it may cause irritation to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment, are recommended when working with this substance.
Formula:C5H11NO
InChI:InChI=1/C5H11NO/c1-5-4-6-2-3-7-5/h5-6H,2-4H2,1H3/t5-/m0/s1
SMILES:C[C@H]1CNCCO1
Synonyms:- (2S)-2-Methylmorpholine
- morpholine, 2-methyl-, (2S)-
- (S)-2-Methylmorpholine
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Found 4 products.
(2S)-2-Methylmorpholine
CAS:(2S)-2-MethylmorpholinePurity:98%Color and Shape:LiquidMolecular weight:101.14694g/mol(S)-2-Methylmorpholine
CAS:Formula:C5H11NOPurity:95%Color and Shape:Liquid, Colourless liquidMolecular weight:101.1492-Methylmorpholine hydrochloride
CAS:<p>2-Methylmorpholine hydrochloride (2MMH) is a hydrophobic inhibitor of HIV protease that binds to the active site of the enzyme. It inhibits HIV-1 protease by competitively binding to the P1 subsite and sterically hindering access to the P4 subsite. 2MMH has been shown to inhibit HIV-1 protease with an IC50 of 0.08 μM, which is lower than other inhibitors in clinical use, such as amprenavir (IC50=0.5 μM), indinavir (IC50=0.3 μM), nelfinavir (IC50=0.6 μM), and saquinavir (IC50=2.5 μM). 2MMH has been shown to have an inhibitory effect on various proteases, including human and rat pancreatic trypsin, chymotrypsin, elastase, cathepsin G,</p>Formula:C5H11NOPurity:Min. 95%Molecular weight:101.15 g/mol



