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1,4-Oxathiin, 2,3-dihydro-6-phenyl- is a chemical compound with the molecular formula C9H10OS. It is a heterocyclic compound, specifically a derivative of oxathiin, which is a sulfur-containing ring structure. This particular compound features a dihydro (two hydrogen atoms added) oxathiin ring and a phenyl group (a benzene ring with a hydrogen atom replaced by an alkyl or aryl group) attached to the 6th position. The presence of the phenyl group imparts unique chemical and physical properties to the molecule, making it potentially useful in various applications, such as pharmaceuticals or materials science.

41803-45-6

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41803-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41803-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41803-45:
(7*4)+(6*1)+(5*8)+(4*0)+(3*3)+(2*4)+(1*5)=96
96 % 10 = 6
So 41803-45-6 is a valid CAS Registry Number.

41803-45-6Relevant academic research and scientific papers

Studies on the Preparation of Dihydro-1,4-oxathiines. Computer-Assisted Evaluation of the Results of Retrosynthetic Analysis Verified by Synthetic Experiments and By-Product Analyses. Synthetic Pathways Involving α-Sulfenylated Ketones and 1,3-Oxathiolanes of α-Halo and α-Hydroxy K...

Nevalainen, Vesa,Pohjala, Esko,Maelkoenen, Pentti,Hukkanen, Heikki

, p. 591 - 602 (2007/10/02)

The preparation of 2- and 2,3-substituted 5,6-dihydro-1,4-oxathiines has been studied by computer simulation and by experiment.Three major synthetic pathways, involving 2-(1-hydroxyalkyl)-1,3-oxathiolanes, 2-(1-haloalkyl)-1,3-oxathiolanes, 2-hydroxyethylthiomethyl ketones, methanesulfonates of 2-hydroxyethylthiomethyl ketones and 2-choroethylthiomethyl ketones as intermediates, were evaluated, by running the program CAMEO, and by experiment.The results of the two approaches were compared and the major by-products of the reactions were identified by GLC/MS.

Studies on the Formation of Dihydro-1,4-oxathiines by Halogenation of 1,3-Oxathiolanes.

Nevalainen, Vesa,Pohjala, Esko

, p. 1401 - 1421 (2007/10/02)

Formation of 5,6-dihydro-1,4-oxathiines (1a-g) by halogenation of 1,3-oxathiolanes (4a-g) was investigated.Moderate yields of (1) were obtained in systems in which the newly formed double bond of the heterocyclic ring was stabilised by conjugation.In addition to the dihydro-1,4-oxathiines (1a-g), their halogenated derivatives and some fused and spiro 1,4-oxathianes were produced as by-products.By-products of reactions were analysed by gas chromatography and mass-spectrometry.

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