Neophyl chloride
Chemical compound / From Wikipedia, the free encyclopedia
Neophyl chloride, C6H5C(CH3)2CH2Cl, is a halogenated organic compound with unusual nucleophilic substitution properties. Neophyl chloride is used to form a versatile organolithium reagent, neophyl lithium, by reaction with lithium.[2][3]
Quick Facts Names, Identifiers ...
Names | |
---|---|
Preferred IUPAC name
(1-Chloro-2-methylpropan-2-yl)benzene | |
Other names
(Chloro-tert-butyl)benzene | |
Identifiers | |
| |
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.007.453 |
EC Number |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C10H13Cl | |
Molar mass | 168.663 g/mol |
Appearance | colorless liquid |
Density | 1.047 g/cm3 |
Boiling point | 223 °C (433 °F; 496 K) |
organic solvents | |
Hazards | |
GHS labelling:[1] | |
Warning | |
H315, H319, H335 | |
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Close