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Organolithium

Organolithium compounds possess direct bonds between carbon and lithium atoms. Organolithium reagents are strongly basic, highly reactive nucleophiles used to transfer organic groups or lithium atoms to substrates during organic synthesis reactions.
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Lithium tri-tert-butoxyaluminum hydride, nominally 1M in THF, packaged under Argon in resealable ChemSeal™ bottles

CAS: 17476-04-9 Molecular Formula: C12H28AlLiO3 MDL Number: MFCD00011532 Synonym: Lithium hydridotris(tert-butoxy)aluminate

CAS 17476-04-9
MDL Number MFCD00011532
Synonym Lithium hydridotris(tert-butoxy)aluminate
Molecular Formula C12H28AlLiO3
2

sec-Butyllithium, 1.3M in cyclohexane, packaged under Argon in resealable ChemSeal™ bottles, Thermo Scientific™

CAS: 598-30-1 Molecular Formula: C4H9Li Molecular Weight (g/mol): 64.06 MDL Number: MFCD00009323 InChI Key: VATDYQWILMGLEW-UHFFFAOYNA-N Synonym: sec-butyllithium,s-buli,s-butyllithium,s-butyl lithium,unii-5yv3gii1tb,lithium, 1-methylpropyl,5yv3gii1tb,secbutyllithium,b-butyllithium,sec-butyllitium PubChem CID: 102446 IUPAC Name: (butan-2-yl)lithium SMILES: [Li]C(C)CC

PubChem CID 102446
CAS 598-30-1
Molecular Weight (g/mol) 64.06
MDL Number MFCD00009323
SMILES [Li]C(C)CC
Synonym sec-butyllithium,s-buli,s-butyllithium,s-butyl lithium,unii-5yv3gii1tb,lithium, 1-methylpropyl,5yv3gii1tb,secbutyllithium,b-butyllithium,sec-butyllitium
IUPAC Name (butan-2-yl)lithium
InChI Key VATDYQWILMGLEW-UHFFFAOYNA-N
Molecular Formula C4H9Li