| Weight | 95.145 g/mol |
|---|---|
| Formula | C6H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2-Azabicyclo[2.2.1]hept-5-ene (6671-85-8)
6671-85-8
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- Sigma-Aldrich - Search for 2-Azabicyclo[2.2.1]hept-5-ene
- Fisher Scientific - Search for 2-Azabicyclo[2.2.1]hept-5-ene
- TCI - Search for 2-Azabicyclo[2.2.1]hept-5-ene
- Regiochemistry of the reductive Heck coupling of 2-azabicyclo[2.2.1]hept-5-ene. Synthesis of epibatidine analogues (Tetrahedron, 1998)
- Synthesis of Epibatidine Isomers: Reductive Heck Coupling of 2-Azabicyclo[2.2.1]hept-5-ene derivatives (Tetrahedron, 1999)
- One-Pot Synthesis of Pentaalkyl 7-[(Alkylamino)carbonyl]-2-oxa-1-azabicyclo[3.2.0]hept-3-ene-3,4,5,6,7-pentacarboxylate (Helvetica Chimica Acta, 2006)
- On-site modification of oligopeptides: Conversion of seryl into (exo)-2-azabicyclo[2.2.1]hept-5-ene-3-carbonyl residues (Tetrahedron Letters, 1995)
- A Novel Skeletal Rearrangement of 2-Azabicyclo(2.2.1)hept-5-ene-3-carboxylic Acid Derivatives into 2-Oxabicyclo(3.3.0)-oct-7-en-3-ones under Acidic Conditions. (Bulletin of the Chemical Society of Japan, 1992)
- Design and synthesis of methyl 2-methyl-7,7-dihalo-5-phenyl-2-azabicyclo[4.1.0]hept-3-ene-4-carboxylates with calcium channel antagonist activity (Bioorganic & Medicinal Chemistry, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 6671-85-8
-
SMILESC1C2CNC1C=C2
-
InChIKeyKPFWYFYRULFDQP-UHFFFAOYSA-N
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Safety
Alternate Names
Estimated Properties
| Boiling Point | 133.49 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 146.61 C | EPI Suite |
| Density | 0.98 g/cm3 | EPA T.E.S.T. |
| Flash Point | 51.26 C | EPA T.E.S.T. |
| Melting Point | -2.84 C | EPI Suite |
| Water Solubility | 98959 mg/L | EPA T.E.S.T. |
| Water Solubility | 82298 mg/L | EPI Suite |
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