Product Name:1-Thia-6-azaspiro[3.3]heptane hydrochloride

IUPAC Name:1-thia-6-azaspiro[3.3]heptane hydrochloride

CAS:1427452-92-3
Molecular Formula:C5H10ClNS
Purity:95%+
Catalog Number:CM534399
Molecular Weight:151.65

Packing Unit Available Stock Price($) Quantity
CM534399-100mg in stock ȃȃǤ
CM534399-250mg in stock ŗƥȃ

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Product Details

CAS NO:1427452-92-3
Molecular Formula:C5H10ClNS
Melting Point:-
Smiles Code:Cl.C1CC2(CNC2)S1
Density:
Catalog Number:CM534399
Molecular Weight:151.65
Boiling Point:
MDL No:
Storage:

Category Infos

Spiro Compounds
A spiro compound is a polycyclic compound in which two monocyclic rings share one carbon atom; the shared carbon atom is called a spiro atom. Spiro compounds have rigid structures, stable structures, and have special properties that general organic compounds do not possess, such as anomeric effect, spiro conjugation and spiro hyperconjugation. Compared with the monocyclic structure or the planar aromatic structure, the spiro structure has a larger three-dimensional structure; the heterocyclic spiro structure is also regarded as the biological isostere of some groups, which can change the drug to a certain extent. The water solubility, lipophilicity, dominant conformation and ADMET properties of the molecule make the optimized lead molecule easier to drug. Therefore, spiro compounds occupy a very important position in drug development.
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Azetidines
Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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Thietanes
Thietanes are important structural motifs of some biological compounds and useful intermediates in organic synthesis.