2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine
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2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine
structure -
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CAS No:
479-59-4
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Formula:
C12H15N
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Chemical Name:
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine
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Synonyms:
1H,5H-Benzo[ij]quinolizine,2,3,6,7-tetrahydro-;Julolidine;2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine;NSC 82354
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CAS No:
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine Basic Attributes
173.25
173.25
139925
207-535-0
8ERL3KJ6GQ
82354
DTXSID0060060
29339900
Characteristics
3.2
2.8
Clear yellow to orange-brown Liquid After Melting
1.1 g/cm3
40 °C
155-156 °C @ Press: 17 Torr
>230 °F
1.568 (25ºC)
soluble in toluene. Insoluble in water.
0-6°C
0.000554mmHg at 25°C
Safety Information
NONH for all modes of transport
3
52/53
24/25-61
Stable under normal temperatures and pressures.
P201, P202, P281, P308+P313, P405, P501
H341
2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine Use and Manufacturing
66.5g (0.5mol) of tetrahydroquinoline and 400g of 1-bromo-3-chloropropane were heated in a 150-160℃ oil bath for 20 hours. After cooling, 50ml of concentrated hydrochloric acid and 500ml of water were added to steam distillation to remove excess 1- Bromo-3-chloropropane. Adjust the residue to alkaline with 40% sodium hydroxide and extract with ether. The ether extract is washed with water, dried with granular sodium hydroxide, distilled to remove the ether, and distilled under reduced pressure to collect the 105-110°C (0.133kPa) fraction to obtain 67-70g of jololidine.
Used in organic synthesis.
1H,5H-Benzo[ij]quinolizine, 2,3,6,7-tetrahydro-: ACTIVE|PMN - indicates a commenced PMN (Pre-Manufacture Notices) substance.
Computed Properties
Molecular Weight:173.25
XLogP3:2.8
Hydrogen Bond Acceptor Count:1
Exact Mass:173.120449483
Monoisotopic Mass:173.120449483
Topological Polar Surface Area:3.2
Heavy Atom Count:13
Complexity:172
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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2,3,6,7-Tetrahydro-1H,5H-benzo[ij]quinolizine
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