CAS 22795-99-9
:(2S)-1-Ethyl-2-pyrrolidinemethanamine
Description:
(2S)-1-Ethyl-2-pyrrolidinemethanamine, with the CAS number 22795-99-9, is an organic compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. This compound features an ethyl group attached to the nitrogen atom of the pyrrolidine, along with a methanamine functional group, contributing to its amine characteristics. It is a chiral molecule, with the (2S) designation indicating the specific stereochemistry at the second carbon of the pyrrolidine ring. This stereochemistry can influence its biological activity and interactions with other molecules. The compound is typically colorless to pale yellow and may be soluble in polar solvents due to the presence of the amine group. Its properties make it of interest in various fields, including medicinal chemistry and drug development, where it may serve as a building block for more complex molecules or as a potential therapeutic agent. Safety data and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use.
Formula:C7H16N2
InChI:InChI=1S/C7H16N2/c1-2-9-5-3-4-7(9)6-8/h7H,2-6,8H2,1H3/t7-/m0/s1
InChI key:InChIKey=UNRBEYYLYRXYCG-ZETCQYMHSA-N
SMILES:C(N)[C@H]1N(CC)CCC1
Synonyms:- (-)-1-Ethyl-2-(aminomethyl)pyrrolidine
- (-)-2-(Aminomethyl)-1-ethylpyrrolidine
- (2S)-1-ethyl-2-Pyrrolidinemethanamine
- (S)-(-)-1-Ethyl-2-pyrrolidinemethanamine
- (S)-(-)-2-Aminomethyl-1-Ethylpyrrolidine
- (S)-(1-Ethylpyrrolidin-2-yl)methanamine
- (S)-N-Ethyl-2-Aminomethyl pyrrolidine
- 1-[(2S)-1-ethylpyrrolidin-2-yl]methanamine
- 2-Pyrrolidinemethanamine, 1-ETHYL-, (2S)-
- 2-Pyrrolidinemethanamine, 1-ethyl-, (S)-
- Aminomethylethylpyrrolidine
- Pyrrolidine, 2-(aminomethyl)-1-ethyl-, (-)-
- S-(-)-1-Ethyl-2-Aminomethylpyrrolidine
- S-(-)-2-(Aminomethyl)-N-ethylpyrrolidine
- S-(-)-N-ETHYL-ALPHA-(Aminomethyl)Pyrrolidine
- S-(-)N-ETHYL-A-Aminomethyl-Pyrrolidine
- S-(-)N-ethyl-2-aminomethylpyrrolidine
- S-(-)N-ethyl-a-aminomethyl-pyrrolidine(s(-)NEAMP)
- [((S)-1-Ethylpyrrolidin-2-yl)methyl]amine
- [(2S)-1-Ethylpyrrolidin-2-yl]methanamine
- See more synonyms
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Found 10 products.
(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine, 95%
CAS:<p>It is used as a pharmaceutical intermediate of antipsychotics levosulpiride and for the preparation of medicines and other fine chemicals. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the</p>Formula:C7H16N2Purity:95%Molecular weight:128.22(S)-(1-Ethylpyrrolidin-2-yl)methanamine
CAS:Formula:C7H16N2Purity:98%Color and Shape:LiquidMolecular weight:128.2153(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine
CAS:Formula:C7H16N2Purity:>98.0%(GC)(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:128.22(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine
CAS:<p>(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine</p>Formula:C7H16N2Purity:98%Color and Shape: light yellow liquidMolecular weight:128.22g/mol(2S)-2-Aminomethyl-1-ethylpyrrolidine
CAS:<p>Applications An impurity found in amisulpride (A633250).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>Formula:C7H16N2Color and Shape:NeatMolecular weight:128.22(2S)-2-Aminomethyl-1-ethylpyrrolidine-d5
CAS:Controlled Product<p>Applications (2S)-2-Aminomethyl-1-ethylpyrrolidine-d5 is the isotope labelled analog of an impurity found in Amisulpride (A633250).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Preuss, J., et al.: J. Med. Chem., 55, 7262 (2012); Sheffler, D.J., et al.: Bioorg. Med. Chem. Lett., 22, 3921 (2012);<br></p>Formula:C7D5H11N2Color and Shape:NeatMolecular weight:133.246(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine
CAS:Formula:C7H16N2Purity:98%Color and Shape:LiquidMolecular weight:128.219(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine
CAS:<p>(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine is a compound that belongs to the class of cyclohexane ring. It has been shown to possess potent anti-infective activity against bacteria and fungi, but not against viruses. It is an inorganic compound that can be synthesized by the chlorination of (S)-(-)-2-aminoethanol. This method is efficient and does not require any organic solvents or catalysts. The binding of inhibitors to the enzyme can be studied by using this molecule as a model system. This molecule also has application as a coating for metal surfaces, which can inhibit corrosion.</p>Formula:C7H16N2Purity:Min. 95%Molecular weight:128.22 g/mol








