Weight | 101.193 g/mol |
---|---|
Formula | C6H15N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
DIISOPROPYLAMINE (110-97-4, 108-18-9)
lithium diisopropylamide · diisopropylamine hydrochloride · N,N-diisopropylamine
Score:
#1363 in Chemistry
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- Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis (Angewandte Chemie, 2007)
- Isocyanide synthesis with phosphoryl chloride and diisopropylamine (Synthesis, 1985)
- Reductions of .alpha.-substituted ketones by lithium diisopropylamide (Journal of Organic Chemistry, 1978)
- Organoselenium chemistry. 4. Deprotonations with potassium diisopropylamide-lithium tert-butoxide. Alkylation of 1-(phenylseleno)alkenes and bis(phenylseleno) acetals (Journal of Organic Chemistry, 1978)
- Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis (Journal of Organic Chemistry, 2009)
- The first structural characterization of a dimeric lithium ketone enolate-lithium diisopropylamide complex (Journal of the American Chemical Society, 1987)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H402: Harmful to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 3 - lithium diisopropylamide
- diisopropylamine hydrochloride
- N,N-diisopropylamine
- diisopropylamine, lithium salt
- Disotat
- diisopropylamine sulfate (2:1)
-
SMILESCC(C)NC(C)C
-
InChIKeyUAOMVDZJSHZZME-UHFFFAOYSA-N
- Pubchem - DIISOPROPYLAMINE
- Wikipedia - diisopropylamine
Diisopropylamine is a secondary amine with the chemical formula (CH3)2HC-NH-CH(CH3)2. It is best known as its lithium derivative of its conjugate base, lithium diisopropylamide, known as "LDA". LDA is a strong, non-nucleophilic base.
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