8-METHYL-8-AZABICYCLO[3.2.1]OCTANE
8-METHYL-8-AZABICYCLO[3.2.1]OCTANE Basic information
- Product Name:
- 8-METHYL-8-AZABICYCLO[3.2.1]OCTANE
- Synonyms:
-
- 8-METHYL-8-AZABICYCLO[3.2.1]OCTANE
- 1alphaH,5alphaH-Tropane
- 2,3-Dihydro-8-methylnortropidine
- 8-Azabicyclo[3.2.1]octane, 8-methyl-
- N-Methyl-8-azabicyclo[3.2.1]octane
- TROPANE
- (1S,5R)-8-Methyl-8-azabicyclo[3.2.1]octane
- (1β,5β)-8-Methyl-8-azabicyclo[3.2.1]octane
- CAS:
- 529-17-9
- MF:
- C8H15N
- MW:
- 125.21
- Product Categories:
-
- Heterocyclic Compounds
- Mol File:
- 529-17-9.mol
8-METHYL-8-AZABICYCLO[3.2.1]OCTANE Chemical Properties
- Boiling point:
- 167-169 °C (lit.)
- Density
- 0.931 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.477(lit.)
- Flash point:
- 108 °F
- form
- liquid
- pka
- 11.57±0.20(Predicted)
- Merck
- 13,9847
- InChI
- 1S/C8H15N/c1-9-7-3-2-4-8(9)6-5-7/h7-8H,2-6H2,1H3/t7-,8+
- InChIKey
- XLRPYZSEQKXZAA-OCAPTIKFSA-N
- SMILES
- CN1[C@H]2CCC[C@@H]1CC2
- LogP
- 1.740 (est)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 10-36/37/38
- Safety Statements
- 16-26-36
- RIDADR
- UN 1993 3/PG 3
- WGK Germany
- 3
- HazardClass
- 3.2
- PackingGroup
- III
- Storage Class
- 3 - Flammable liquids
- Hazard Classifications
- Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3
MSDS
- Language:English Provider:SigmaAldrich
8-METHYL-8-AZABICYCLO[3.2.1]OCTANE Usage And Synthesis
Uses
Tropane (8-methyl-8-azabicyclo[3.2.1]-octane) is a bridged bicyclic N-containing compound. The 8-methyl-8-azabicyclo[3.2.1]-octane has a tropane ring system, which is an important substructure in a number of natural products and synthetic compounds of biological and medicinal importance. Production of tropane alkaloid in callus and root cultures of seven Hyoscyamus species has been studied. Tropane derivatives are reported to undergo rapid N-methyl inversion.
General Description
Tropane (8-methyl-8-azabicyclo[3.2.1]-octane) is a bridged bicyclic N-containing compound. The 8-methyl-8-azabicyclo[3.2.1]-octane has a tropane ring system, which is an important substructure in a number of natural products and synthetic compounds of biological and medicinal importance. Production of tropane alkaloid in callus and root cultures of seven Hyoscyamus species has been studied. Tropane derivatives are reported to undergo rapid N-methyl inversion.
8-METHYL-8-AZABICYCLO[3.2.1]OCTANE Preparation Products And Raw materials
Preparation Products
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8-METHYL-8-AZABICYCLO[3.2.1]OCTANE(529-17-9)Related Product Information
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