147441-52-9

Basic information

• Product Name: (2S)-2-(4-bromophenyl)-1,3-oxathiolane
• CAS NO: 147441-52-9
• Molecular Formula: C₉H₉BrOS
• Molecular Weight: 245.1362
• Mol File: 147441-52-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 339.1°C at 760 mmHg
• Flash Point: 158.9°C
• Density: 1.535g/cm³
• Vapor Pressure: 0.000185mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: (2S)-2-(4-bromophenyl)-1,3-oxathiolane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-(4-bromophenyl)-1,3-oxathiolane(147441-52-9)
• EPA Substance Registry System: (2S)-2-(4-bromophenyl)-1,3-oxathiolane(147441-52-9)

Safety Data

• Hazardous Substances Data: 147441-52-9(Hazardous Substances Data)

Usage

General Description

(2S)-2-(4-bromophenyl)-1,3-oxathiolane is a chemical compound with the molecular formula C8H7BrOS. It is a chiral molecule, meaning it has two possible stereoisomeric forms, with the (2S) configuration being the specific form described. The compound contains a six-membered heterocyclic ring consisting of oxygen, sulfur, and carbon atoms, with a bromophenyl group attached to one of the carbon atoms. (2S)-2-(4-bromophenyl)-1,3-oxathiolane has potential applications in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its unique chemical structure and properties make it a subject of interest in the field of medicinal chemistry.

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 60-24-2 2-hydroxyethanethiol 

Downstream Products

• 873-75-6 4-bromobenzenemethanol 
• 1186296-22-9 dibenzyl (2R)-2-(4-bromophenyl)-1,4-oxathiane-3,3-dicarboxylate 
• 1122-91-4 4-bromo-benzaldehyde 
• 83521-65-7 2-(4-bromophenyl)-1,3-dithiolane 
• 876156-57-9 2-(4-bromophenyl)-3-trifluoromethyl-1,4-oxathiinane-3-carboxylic acid methyl ester 
• 876156-57-9 2-(4-bromophenyl)-3-trifluoromethyl-1,4-oxathiinane-3-carboxylic acid methyl ester 

Relevant articles and documents

Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones

In synthetic chemistry, the protection of aldehydes and ketones is crucial during multistep synthesis of complex molecules. Organic chemists have paid substantial attention to the synthesis of 1,3-oxathiolanes and 1,3-oxathianes because of their considera

Nickel(II) chloride hexahydrate catalyzed reaction of aromatic aldehydes with 2-mercaptoethanol: Formation of supramolecular helical assemblage of the product

Various aromatic aldehydes on reaction with 2-mercaptoethanol provided an unanticipated product, bis(2-hydroxyethyl)dithioacetals (3) as the major product along with the expected product 1,3-oxathiolanes (4) in the presence of 0.05 equiv amount of nickel(

Melamine trisulfonic acid as a new, efficient and reusable catalyst for the chemoselective oxathioacetalyzation of aldehydes

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