4-amino-1-benzylpyrrolidin-2-one dihydrochloride

4-amino-1-benzylpyrrolidin-2-one dihydrochloride

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

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

tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride

$250.00
CAS No.: 2102410-18-2
Catalog No.: 193009
Purity: 95%
MF: C10H21ClN2O2
MW: 236.743
Storage: 2-8 degree Celsius
SMILES: Cl.C[C@H]1[C@H](CNC1)NC(OC(C)(C)C)=O
Availability:
In stock
SKU
193009
  • Size
    Price
    Stock
    Estimated Shipping Time
tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride; CAS No.: 2102410-18-2; tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride. PROPERTIES: This compound presents as a white crystalline powder with molecular formula C10H18N2O2 {HCl and a molecular weight of 220.72 g/mol. It demonstrates a melting point in the range of 142-146 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. 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 tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride serves as a key intermediate for synthesizing antidepressant agents, as documented in pharmaceutical research focusing on serotonergic compounds. Its methyl substituent enables improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with insecticidal activities through formation of urea derivatives. 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.

Reviews

Write Your Own Review
You're reviewing:tert-butyl (3R,4R)-4-methylpyrrolidin-3-ylcarbamate hydrochloride
Your Rating