cis-cyclopentane-1,2-diamine dihydrochloride
$371.00
CAS No.: 310872-08-3
Catalog No.: 195925
Purity: 95%
MF: C5H14Cl2N2
MW: 173.087
Storage: 2-8 degree Celsius
SMILES: Cl.Cl.[C@@H]1([C@H](CCC1)N)N
Catalog No.: 195925
Purity: 95%
MF: C5H14Cl2N2
MW: 173.087
Storage: 2-8 degree Celsius
SMILES: Cl.Cl.[C@@H]1([C@H](CCC1)N)N
cis-cyclopentane-1,2-diamine dihydrochloride; CAS No.: 310872-08-3; cis-cyclopentane-1,2-diamine dihydrochloride. PROPERTIES: cis-Cyclopentane-1,2-diamine dihydrochloride has molecular formula C5H10N2 {2HCl, giving it a molecular weight of 169.06 g/mol. It appears as a white crystalline powder with a melting point between 195-198 C. The compound demonstrates good chemical stability under standard conditions but is hygroscopic. Recommended storage involves keeping it in a tightly sealed container at room temperature (15-25 C) with desiccants. Safety data indicates it may cause respiratory irritation and requires use of chemical splash goggles and lab coats during handling. The compound has a logP value of approximately 0.5 and exhibits high aqueous solubility. APPLICATIONS: This cis-cyclopentane-1,2-diamine dihydrochloride is extensively used in the synthesis of antimicrobial agents. Its cyclopentane-diamine structure provides a platform for developing antibacterial agents targeting bacterial dihydrofolate reductase. A study in Antimicrobial Agents and Chemotherapy highlighted its role in creating antibacterial agents with activity against methicillin-resistant Staphylococcus aureus (MRSA). In pharmaceutical applications, it serves as a building block for synthesizing kinase inhibitors. The diamine groups provide steric and electronic effects beneficial for optimizing kinase hinge binding. Research in the Journal of Medicinal Chemistry demonstrated its utility in developing JAK3 inhibitors for autoimmune disease therapy. Additionally, the compound is utilized in the preparation of fluorescent probes. The amine groups provide sites for installing fluorescence tags, enabling detection of enzymatic activity in biological systems, as reported in Bioconjugate Chemistry.
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