14109-98-9

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 7 carbon (C), 10 hydrogen (H), 2 nitrogen (N), 1 oxygen (O), and 1 sulfur (S) atoms.

Explanation

A spiro compound is a type of organic compound that contains two rings connected by a single atom. In this case, the compound has a spiro ring system with two nitrogen atoms and a five-membered ring structure.

Explanation

The compound contains two nitrogen atoms, which are part of the spiro ring system.

Explanation

The compound contains one sulfur atom, which is part of the 2-thio functional group.

Explanation

The compound has a five-membered ring structure, which is a common feature in many organic compounds and can influence their chemical properties.

Explanation

The compound is often used in organic synthesis as a building block for the development of new drugs and compounds due to its unique structural properties.

Explanation

The compound is used in pharmaceutical research to develop new drugs and biologically active molecules, taking advantage of its versatile structure and potential for functional group transformations.

Explanation

The compound's spiro ring system and the potential for functional group transformations make it a valuable starting material for the preparation of diverse molecular structures.

Explanation

Due to its unique structure and potential for functional group transformations, the compound has the potential to be used in the development of biologically active molecules, which could have applications in medicine and pharmaceuticals.

Spiro compound

Yes

Nitrogen atoms

2

Sulfur atom

1

Five-membered ring structure

Yes

Application in organic synthesis

Yes

Application in pharmaceutical research

Yes

Versatile starting material

Yes

Biological activity

Potential

Upstream product

• 859743-19-4 4-(2-hydroxy-ethylamino)-1,3-diaza-spiro[4.4]non-3-ene-2-thione 
• 859743-19-4 4-[(Z)-2-Hydroxy-ethylimino]-1,3-diaza-spiro[4.4]nonane-2-thione 
• 17356-08-0 thiourea 
• 52-52-8 1-amino-1-cyclopentanecarboxylic acid 
• 23000-19-3 5,5-pentamethylene-2,4-dithiohydantoin 
• 5699-93-4 cycloheptanespiro-4'-imidazolidine-2',5'-dithione 
• 5626-12-0 cyclooctanespiro-4'-imidazolidine-2',5'-dithione 
• 70014-46-9 5,5-Cycloundecamethylene-2,4-dithiohydantoin 
• 83521-99-7 cyclopentanespiro-4'-imidazolidine-2',5'-dithione 
• 699-51-4 1,3-diazaspiro[4.4]nonane-2,4-dione 

Downstream Products

• 934223-89-9 benzyl 2-amino-1,3-diazaspiro[4.4]non-1-en-4-ol-3-carboxylate 
• 934223-88-8 benzyl 1,3-diaza-2-(methylthio)spiro[4.4]non-1-en-4-ol-3-carboxylate 
• 934223-91-3 benzyl 1,3-diaza-2-(methylthio)spiro[4.4]non-1-en-4-one-3-carboxylate 
• 934223-86-6 1,3-diaza-2-methylthio-3-(4-methoxybenzenesulfonyl)spiro[4.4]non-1-en-4-one 
• 934223-82-2 1,3-diaza-2-methylthio-4-(phenylmethoxy)spiro[4.4]non-1-ene 

Relevant academic research and scientific papers

Two cycloalkanespiro-5-(2-thiohydantoins): Synthesis, spectral and structural characterization

The presented study deals with the structural and spectral properties of two derivatives of 2-thiohydantoin employing experimental and theoretical methods. The crystal structures of two novel cycloalkanespiro-5-(2-thiohydantoins) are described and compare

Two methods for spirothiohydantoin synthesis

Two methods for spirothiohydantoin synthesis are presented. The title compounds were prepared with reaction of the corresponding 1- aminocycloalkanecarboxylic acids and thiourea. These compounds were also prepared by a hydrolysis of the relevant spirodithiohydantoins with barium hydroxide. The structures of the compounds obtained were verified by comparison of 1H, and 13C NMR, IR and MS spectral data.

Evaluation of strategies for the synthesis of the guanidine hemiaminal portion of palau'amine

Potential methods for the generation of the guanidine hemiaminal functionality of palau'amine (1) from a spirocyclic thiohydantoin precursor are examined using a spirobicyclic model system, culminating in the identification of an efficient means of effect

Synthesis, spectroscopic characterization and ab initio investigation of thioanalogues of spirohydantoins

Dithioanalogues of cycloalkanespiro-5-hydantoins were prepared by reaction of the respective spirohydantoins with Lawesson's reagent or P4S 10. Cycloalkanespiro-5-(2-thiohydantoins) and cycloalkanespiro-5-(4- hydantoins) were also synthesized from cycloalkanespiro-5-(2,4-dithiohydantoins) via different reaction pathways. The structures of the compounds obtained were verified by 1H, 13C NMR and IR spectroscopy. Quantum-chemical calculations at the ab initio level of molecular nonlinear characteristics were performed. Increase of polarizability α and the second hyperpolarizability ? with enlarging the saturated ring was observed in all the structures studied.