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1-Aminomethylindane

From Wikipedia, the free encyclopedia
1-Aminomethylindane
Names
IUPAC name
2,3-dihydro-1H-inden-1-ylmethanamine
Other names
1-AMI
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
EC Number
  • 832-793-1
  • InChI=1S/C10H13N/c11-7-9-6-5-8-3-1-2-4-10(8)9/h1-4,9H,5-7,11H2
    Key: QBHALBZXAXQBOY-UHFFFAOYSA-N
  • C1CC2=CC=CC=C2C1CN
Properties
C10H13N
Molar mass147.221 g·mol−1
Hazards
GHS labelling:[1]
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H302,H315,H318,H335
P261,P264,P264+P265,P270,P271,P280,P301+P317,P302+P352,P304+P340,P305+P354+P338,P317,P319,P321,P330,P332+P317,P362+P364,P403+P233,P405,P501
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

1-Aminomethylindane (1-AMI) is achemical compound andderivative ofindane. It can also be thought of as acyclized phenethylamine orβ-phenethylamine derivative in which theside chain iscyclized with thebenzenering. 1-AMI is theparent compound of a group ofpsychedelic- andentactogen-relateddrugs that includes1-aminomethyl-5-methoxyindane (1-AMMI; related topara-methoxyamphetamine (PMA)),2CB-Ind (related to2C-B),jimscaline (related tomescaline), andbromojimscaline (related to2-bromomescaline).[1][2][3]

See also

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References

[edit]
  1. ^Trachsel, D.; Lehmann, D.; Enzensperger, C. (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved31 January 2025.
  2. ^Blaazer AR, Smid P, Kruse CG (September 2008). "Structure-activity relationships of phenylalkylamines as agonist ligands for 5-HT(2A) receptors".ChemMedChem.3 (9):1299–1309.doi:10.1002/cmdc.200800133.PMID 18666267.
  3. ^McLean TH, Chambers JJ, Parrish JC, Braden MR, Marona-Lewicka D, Kurrasch-Orbaugh D, Nichols DE (July 2006). "C-(4,5,6-trimethoxyindan-1-yl)methanamine: a mescaline analogue designed using a homology model of the 5-HT2A receptor".J Med Chem.49 (14):4269–4274.doi:10.1021/jm060272y.PMID 16821786.
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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