| Weight | 115.18 g/mol |
|---|---|
| Formula | C5H13N3 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,1,3,3-Tetramethylguanidine (1729-17-5, 80-70-6)
Score:
#6798 in Chemistry
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- Direct aldol reactions catalyzed by 1,1,3,3-tetramethylguanidine lactate without solvent (Green Chemistry, 2005)
- Catalytic cyanosilylation of ketones using organic catalyst 1,1,3,3-tetramethylguanidine (Tetrahedron Letters, 2006)
- Synthesis and SO2 absorption/desorption properties of poly (1,1,3,3 -tetramethylguanidine acrylate) (Macromolecules, 2007)
- Preparation of room-temperature ionic liquids by neutralization of 1,1,3,3-tetramethylguanidine with acids and their use as media for mannich reaction (Synthetic Communications, 2004)
- PtII-Mediated NitrileTetramethylguanidine Coupling as a Key Step for a Novel Synthesis of 1,6-Dihydro-1,3,5-triazines (Inorganic Chemistry, 2007)
- Preparation and SO2 Absorption/Desorption Properties of Crosslinked Poly(1,1,3,3-Tetramethylguanidine Acrylate) Porous Particles (Macromolecular Rapid Communications, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN(C)C(=N)N(C)C
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InChIKeyKYVBNYUBXIEUFW-UHFFFAOYSA-N
- Pubchem - 1,1,3,3-Tetramethylguanidine
- Wikipedia - 1,1,3,3-tetramethylguanidine
Tetramethylguanidine is an organic compound with the formula HNC(N(CH3)2)2. This colourless liquid is a strong base with a higher pKa than typical amines. It was originally prepared from tetramethylthiourea via S-methylation and amination, but alternative methods start from cyanogen iodide.
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Synthesis
Methylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
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1,1,3,3-Tetramethylguanidine
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