| Weight | 163.205 g/mol |
|---|---|
| Formula | C6H18N3P |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Hexamethylphosphorous triamide (1608-26-0)
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- C6 substitution of inosine using hexamethylphosphorous triamide in conjunction with carbon tetrahalide or N-halosuccinimide (Tetrahedron Letters, 2000)
- Synthetic Methods and Reactions; 551. Novel Conversion of Primary Aliphatic and Arylaliphatic Nitro Compounds into Nitriles with Trimethyl(ethyl)amine/ Sulfur Dioxide Complexes or Hexamethylphosphorous Triamide (Synthesis, 1979)
- The reaction of arylaldehydes with hexamethylphosphorous triamide and the use of the resulting products for the synthesis of enamines and deoxybenzoins (Synthesis, 1991)
- Prostaglandin analog synthesis using hexamethylphosphorous triamide Alkenylcuprate(I) (Prostaglandins, 1974)
- Adducts of hexamethylphosphorous triamide and polyhalo compounds (1954)
- Reaction of hexamethylphosphorous triamide with cotton cellulose (Journal of Applied Polymer Science, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN(C)P(N(C)C)N(C)C
-
InChIKeyXVDBWWRIXBMVJV-UHFFFAOYSA-N
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Hexamethylphosphorous triamide
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