(3S,4R)-4-phenylpyrrolidine-3-carboxylic acid hydrochloride

(3S,4R)-4-phenylpyrrolidine-3-carboxylic acid hydrochloride

(trans)-2,5-dimethylpyrrolidine hydrochloride

(trans)-2,5-dimethylpyrrolidine hydrochloride

(S)-N-methyl(pyrrolidin-2-yl)methanamine

$200.00
CAS No.: 110638-61-4
Catalog No.: 192979
Purity: 95%
MF: C6H14N2
MW: 114.192
Storage: 2-8 degree Celsius
SMILES: CNC[C@H]1NCCC1
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(S)-N-methyl(pyrrolidin-2-yl)methanamine; CAS No.: 110638-61-4; (S)-N-methyl(pyrrolidin-2-yl)methanamine. PROPERTIES: This compound appears as a colorless to pale yellow oil with molecular formula C6H13N2 and a molecular weight of 115.18 g/mol. It has a boiling point in the range of 155-160 C at 760 mmHg and demonstrates good solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to oxidation and should be stored under inert atmosphere. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as (S)-N-methyl(pyrrolidin-2-yl)methanamine may cause skin irritation. The amine group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, (S)-N-methyl(pyrrolidin-2-yl)methanamine serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its chiral amine substituent enables formation of bioactive amides through amidation reactions. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrrolidine ring system also facilitates coordination with metal ions, making it valuable for creating luminescent materials in materials science applications, as evidenced by inorganic chemistry publications.

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