gptkbp:instanceOf
|
gptkb:chemical_compound
organometallic compound
|
gptkbp:category
|
organomagnesium compounds
reagents for organic chemistry
|
gptkbp:contains
|
magnesium
halide
alkyl group
|
gptkbp:discoveredBy
|
gptkb:Victor_Grignard
|
gptkbp:discoveredIn
|
1900
|
gptkbp:example
|
ethylmagnesium chloride
methylmagnesium bromide
phenylmagnesium bromide
|
gptkbp:generalFormula
|
R-Mg-X
|
https://www.w3.org/2000/01/rdf-schema#label
|
Grignard reagent
|
gptkbp:namedAfter
|
gptkb:Victor_Grignard
|
gptkbp:NobelPrizeYear
|
Victor Grignard Nobel Prize in Chemistry 1912
|
gptkbp:requires
|
anhydrous conditions
|
gptkbp:sensitivity
|
moisture
|
gptkbp:solvent
|
Ether
|
gptkbp:stateAtRoomTemperature
|
gptkb:government_agency
|
gptkbp:type
|
gptkb:water
carbonyl compounds
|
gptkbp:usedFor
|
formation of carbon-carbon bonds
|
gptkbp:usedIn
|
organic synthesis
|
gptkbp:usedToPrepare
|
ketones
primary alcohols
alcohols
carboxylic acids
secondary alcohols
tertiary alcohols
|
gptkbp:bfsParent
|
gptkb:Reagent
gptkb:Phenylmagnesium_chloride
|
gptkbp:bfsLayer
|
6
|