5418-11-1

Basic information

• Product Name: PHENYL TRANS-STYRYL SULFONE 99
• Synonyms: PHENYL TRANS-STYRYL SULFONE 99;[2-(Phenylsulfonyl)vinyl]benzene;2-Phenylethenyl phenyl sulfone;Phenyl styryl sulfone;Styryl phenyl sulfone;β-(Phenylsulfonyl)styrene
• CAS NO: 5418-11-1
• Molecular Formula: C₁₄H₁₂O₂S
• Molecular Weight: 244.31
• Product Categories: Organic Building Blocks;Sulfones;Sulfur Compounds
• Mol File: 5418-11-1.mol
• Article Data: 18

Chemical Properties

• Melting Point: 74-75 °C(lit.)
• Boiling Point: 438.2°Cat760mmHg
• Flash Point: 275.1°C
• Appearance: /
• Density: 1.221g/cm³
• CAS DataBase Reference: PHENYL TRANS-STYRYL SULFONE 99(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYL TRANS-STYRYL SULFONE 99(5418-11-1)
• EPA Substance Registry System: PHENYL TRANS-STYRYL SULFONE 99(5418-11-1)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 5418-11-1(Hazardous Substances Data)

Usage

General Description

PHENYL TRANS-STYRYL SULFONE 99 is a chemical compound that contains a phenyl group, a trans-styryl group, and a sulfone functional group. It is a high-purity form of the compound and is often used in the production of various materials and products, including plastics, pharmaceuticals, and organic synthesis. PHENYL TRANS-STYRYL SULFONE 99 is known for its stability and versatility, making it a valuable building block in organic chemistry. Additionally, it is used in the pharmaceutical industry for the synthesis of potential drug candidates due to its unique chemical structure and reactivity. Overall, PHENYL TRANS-STYRYL SULFONE 99 is a key chemical that finds applications in various industries and plays a crucial role in the development of new materials and pharmaceuticals.

Upstream product

• 17872-92-3 (phenylsulfonylmethyl)trimethylsilane 
• 100-52-7 benzaldehyde 
• 100-42-5 styrene 
• 120-72-9 indole 
• 873-55-2 sodium benzenesulfonate 
• 98-85-1 1-Phenylethanol 
• 618-41-7 Benzenesulfinic acid 
• 103-64-0 bromostyrene 
• 140-10-3 (E)-3-phenylacrylic acid 
• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 591-50-4 iodobenzene 
• 677-25-8 ethylenesulfonyl fluoride 
• 5535-48-8 PVS 
• 369-57-3 benzenediazonium tetrafluoroborate 

Downstream Products

• 69333-48-8 1-phenyl sulphonyl-2-methoxy-2-phenyl ethane 
• 18436-04-9 phenyl(β-phenyl sulphenyl-β-phenyl ethyl)sulphone 
• 91152-57-7 C₁₇H₁₉NO₄S 
• 26995-39-1 (1RS,2SR)-1,2-epoxy-2-phenylethyl phenyl sulfone 
• 97764-03-9 C₁₇H₁₉NO₄S 
• 70941-85-4 1-<(E)-2-Phenyl-1-phenylsulfonyl-1-ethenyl>-cyclohexanol 
• 65885-20-3 (2-benzenesulfonyl-1-phenyl-ethyl)-dimethyl-amine 
• 30246-74-3 {[(1E)-1-phenylprop-1-en-2-yl]sulfonyl}benzene 
• 170642-39-4 (2S,5R)-2-((R)-2-Benzenesulfonyl-1-phenyl-ethyl)-3,6-diethoxy-5-isopropyl-2,5-dihydro-pyrazine 
• 170899-20-4 (2S,5R)-2-((S)-2-Benzenesulfonyl-1-phenyl-ethyl)-3,6-diethoxy-5-isopropyl-2,5-dihydro-pyrazine 
• 100-42-5 styrene 
• 108-98-5 thiophenol 
• 27846-25-9 1-phenyl-2-(phenylsulfonyl)ethane 
• 873-55-2 sodium benzenesulfonate 

Relevant articles and documents

Sodium iodide-mediated synthesis of vinyl sulfides and vinyl sulfones with solvent-controlled chemical selectivity

Vinyl sulfides and vinyl sulfones are ubiquitous structures in organic chemistry because of their presence in natural and biologically active compounds and are very frequently encountered structural motifs in organic synthesis. Herein we report an efficie

Visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones

Herein we report a mild, general protocol for visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones. The protocol permits efficient functionalization of sulfones with a broad range of cyclic and acyclic secondary and tert

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Based on the acid-base mixed-ligand assembly strategy, a stable Mn(II)-based metal-organic framework (denoted as Mn-MOFs), containing 1-D Mn–O–C rod-shaped chains, was hydrothermally synthesized and structurally characterized. This material was demonstrated to be an efficient heterogeneous catalyst for the decarboxylative sulfonylation of cinnamic acids with sodium benzene sulfinates. Moreover, the Mn-MOF catalyst could be recycled up to six times with the retention of both catalytic activity and crystal structure.