Nom du produit:1,4-Dioxa-7-thiaspiro[4.4]nonane

IUPAC Name:1,4-dioxa-7-thiaspiro[4.4]nonane

CAS:176-35-2
Formule moléculaire:C6H10O2S
Pureté:95%
Numéro de catalogue:CM211848
Poids moléculaire:146.2

Unité d'emballage Stock disponible Prix($) Quantité
CM211848-5g in stock ǫǑȯ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:176-35-2
Formule moléculaire:C6H10O2S
Point de fusion:-
Code SMILES:O1CCOC12CSCC2
Densité:
Numéro de catalogue:CM211848
Poids moléculaire:146.2
Point d'ébullition:244.7°C at 760 mmHg
N° Mdl:
Stockage:Store at 2-8°C.

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.
Spiro And Bicyclic Compound
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Dioxolanes
Dioxolane is a heterocyclic acetal with the formula (CH2)2O2CH2. It is related to tetrahydrofuran by exchanging an oxygen for the CH2 group. The isomer 1,2-dioxolane (in which the two oxygen centers are adjacent) is a peroxide. 1,3-Dioxolane is used as solvent and comonomer in polyacetal. The dioxolane-type and their hydrogenolysis can provide very valuable partially protected building blocks either for oligosaccharide syntheses or sugar transformations.
Tetrahydrothiophenes
Tetrahydrothiophene is a sulfur-containing saturated heterocyclic compound obtained by catalytic hydrogenation of thiophene. After thiophene is reduced to tetrahydrothiophene, it no longer has a conjugated system and aromaticity. Therefore, tetrahydrothiophene shows the properties of general thioethers. Easily oxidized to sulfoxides and sulfones. Tetrahydrothiophene can be used as a raw material for the production of pharmaceuticals, pesticides and photochemicals.