VINYL PHENYL SULFONE
Phenyl vinyl sulfone
CAS: 5535-48-8
Molecular Formula: C8H8O2S
VINYL PHENYL SULFONE - Names and Identifiers
| Name | Phenyl vinyl sulfone |
| Synonyms | Poly vinyl sulfone Phenyl vinyl sulfone VINYL PHENYL SULFONE Phenyl vinyl sulphone (ethenesulfonyl)benzene 1-(Phenylsulfonyl)ethene (ethenylsulfonyl)benzene Eletriptan intermediate 1 Benzene, (ethenylsulfonyl)- 1,1'-Sulfonylbis(ethene-1,1-diyl)dibenzene |
| CAS | 5535-48-8 |
| EINECS | 226-890-2 |
| InChI | InChI=1/C8H8O2S/c1-2-11(9,10)8-6-4-3-5-7-8/h2-7H,1H2 |
| InChIKey | UJTPZISIAWDGFF-UHFFFAOYSA-N |
VINYL PHENYL SULFONE - Physico-chemical Properties
| Molecular Formula | C8H8O2S |
| Molar Mass | 168.21 |
| Density | 1.2660 (rough estimate) |
| Melting Point | 67-69 °C (lit.) |
| Boling Point | 267.16°C (rough estimate) |
| Flash Point | 178.6°C |
| Solubility | It is soluble in most common organic solvents. |
| Vapor Presure | 0.000864mmHg at 25°C |
| Appearance | White to light brown powder |
| Color | White |
| BRN | 1906894 |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| Refractive Index | 1.5090 (estimate) |
| MDL | MFCD00007554 |
| Use | Commonly used in a variety of cycloaddition reactions to form cyclopropane, cyclohexene and cyclooctadiene compounds |
VINYL PHENYL SULFONE - Risk and Safety
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact R41 - Risk of serious damage to eyes R37/38 - Irritating to respiratory system and skin. R22 - Harmful if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
| HS Code | 29309090 |
VINYL PHENYL SULFONE - Reference Information
| NIST chemical information | information provided by: webbook.nist.gov (external link) |
| uses | is commonly used in a variety of cycloaddition reactions to form cyclopropane, cyclohexene and cyclooctadiene compounds. |
Last Update：2024-04-09 02:00:09
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