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

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

4-(2-bromophenyl)pyrrolidin-2-one

4-(2-bromophenyl)pyrrolidin-2-one

(trans)-2,5-dimethylpyrrolidine hydrochloride

$225.00
CAS No.: 114143-75-8
Catalog No.: 192980
Purity: 95%
MF: C6H14ClN
MW: 135.638
Storage: 2-8 degree Celsius
SMILES: Cl.C[C@@H]1N[C@H](CC1)C
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(trans)-2,5-dimethylpyrrolidine hydrochloride; CAS No.: 114143-75-8; (trans)-2,5-dimethylpyrrolidine hydrochloride. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C6H13N {HCl and a molecular weight of 129.63 g/mol. It demonstrates a melting point in the range of 188-192 C and shows good solubility in water and common polar solvents like methanol. The substance is hygroscopic and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at room temperature with protection from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as (trans)-2,5-dimethylpyrrolidine hydrochloride may cause skin and eye irritation. The pyrrolidine ring requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, (trans)-2,5-dimethylpyrrolidine hydrochloride serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on pyrrolidine derivatives. Its dimethyl substituents enable improved lipophilicity for enhanced membrane permeability. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through formation of urea derivatives. Academic research has 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 coordination polymers in materials science applications, as evidenced by structural chemistry publications.

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