Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C8H15N |
| Molecular Weight | 125.2114 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CC2CCCCN2C1
InChI
InChIKey=HAJKHJOABGFIGP-UHFFFAOYSA-N
InChI=1S/C8H15N/c1-2-6-9-7-3-5-8(9)4-1/h8H,1-7H2
| Molecular Formula | C8H15N |
| Molecular Weight | 125.2114 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Consecutive cyclization of allylaminoalkene by intramolecular aminolithiation-carbolithiation. | 2008 Aug 21 |
|
| Organocatalytic approach to enantioselective one-pot synthesis of pyrrolidine, hexahydropyrrolizine, and octahydroindolizine core structures. | 2009 May 7 |
|
| Methyl 9-p-tolyl-8a,9,9a,10,11,12,13,14a-octa-hydro-8H-benzo[f]chromeno[3,4-b]indolizine-8a-carboxyl-ate. | 2009 Nov 25 |
|
| New one-pot methodologies for the modification or synthesis of alkaloid scaffolds. | 2010 Aug 24 |
|
| (6S,7S,8R,8aS)-6-Ethyl-perhydro-indolizine-7,8-diol. | 2010 Jun 16 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:41:29 GMT 2023
by
admin
on
Sat Dec 16 08:41:29 GMT 2023
|
| Record UNII |
4FG58K748F
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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13618-93-4
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26136
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Indolizidine
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4FG58K748F
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DTXSID40929286
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237-103-7
Created by
admin on Sat Dec 16 08:41:29 GMT 2023 , Edited by admin on Sat Dec 16 08:41:29 GMT 2023
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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ENANTIOMER -> RACEMATE |
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