213306
Phenyl vinyl sulfoxide
95%
About This Item
Productos recomendados
assay
95%
form
liquid
refractive index
n20/D 1.585 (lit.)
bp
93-95 °C/0.2 mmHg (lit.)
density
1.139 g/mL at 25 °C (lit.)
functional group
sulfoxide
storage temp.
2-8°C
SMILES string
C=CS(=O)c1ccccc1
InChI
1S/C8H8OS/c1-2-10(9)8-6-4-3-5-7-8/h2-7H,1H2
Inchi Key
MZMJHXFYLRTLQX-UHFFFAOYSA-N
Gene Information
human ... LOC129293(129293)
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General description
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Artículos
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
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