Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H19NO2.ClH |
Molecular Weight | 257.756 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC2=C(C=C1OC)C(C)N(C)CC2
InChI
InChIKey=LARXMHOYLNCTFD-UHFFFAOYSA-N
InChI=1S/C13H19NO2.ClH/c1-9-11-8-13(16-4)12(15-3)7-10(11)5-6-14(9)2;/h7-9H,5-6H2,1-4H3;1H
Molecular Formula | C13H19NO2 |
Molecular Weight | 221.2955 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Tetrahydroisoquinoline and beta-carboline alkaloids from Haloxylon articulatum (Cav.) Bunge (Chenopodiaceae). | 2003 Jul-Aug |
|
N-Methyl-isosalsoline from Hammada scoparia. | 2008 Aug 6 |
|
Molluscicidal activity of Hammada scoparia (Pomel) Iljin leaf extracts and the principal alkaloids isolated from them against Galba truncatula. | 2009 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:13:34 GMT 2023
by
admin
on
Sat Dec 16 09:13:34 GMT 2023
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Record UNII |
V677TLE007
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Record Status |
Validated (UNII)
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Record Version |
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22645
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DTXSID40974074
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V677TLE007
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6266-98-4
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5852-92-6
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Related Record | Type | Details | ||
---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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PARENT -> SALT/SOLVATE | |||
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ENANTIOMER -> RACEMATE | |||
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SOLVATE->ANHYDROUS |