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A59522

Sigma-Aldrich

2-Aminoindan hydrochloride

98%

Synonym(s):

2-Indanamine hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C9H11N · HCl
CAS Number:
2338-18-3
Molecular Weight:
169.65
Beilstein:
3913700
EC Number:
219-048-0
MDL number:
MFCD00012549
UNSPSC Code:
12352100
PubChem Substance ID:
24891039
NACRES:
NA.22

Assay

98%

form

crystals

mp

245-247 °C (lit.)

SMILES string

Cl[H].NC1Cc2ccccc2C1

InChI

1S/C9H11N.ClH/c10-9-5-7-3-1-2-4-8(7)6-9;/h1-4,9H,5-6,10H2;1H

InChI key

XEHNLVMHWYPNEQ-UHFFFAOYSA-N

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Application

Prepared from 2-indanols via azide displacement and subsequent hydrogenation.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tetrahedron, 61, 6801-6801 (2005)
Sebastian A Andujar et al.
Bioorganic & medicinal chemistry, 16(6), 3233-3244 (2008-01-02)
Brain dopaminergic system has a crucial role in the etiology of several neuropsychiatric disorders, including Parkinson's disease, depression, and schizophrenia. Several dopaminergic drugs are used to treat these pathologies, but many problems are attributed to these therapies. Within this context
J G Cannon et al.
Journal of medicinal chemistry, 25(12), 1442-1446 (1982-12-01)
Two series of N-substituted 2-aminoindan systems have been prepared: 4,5-dihydroxy-2-aminoindan (1) has a hydroxylation pattern analogous to the alpha conformer of dopamine, and 5,6-dihydroxy-2-aminoindan (2) has a hydroxylation pattern of the beta conformer of dopamine. All members of both series
R A Glennon et al.
Pharmacology, biochemistry, and behavior, 21(6), 895-901 (1984-12-01)
Animals (rats) trained to discriminate 1.0 mg/kg of S(+)-amphetamine sulfate from saline, using a standard operant training procedure, were administered doses of various amphetamine analogs in tests of stimulus generalization in order to study structure-activity relationships (SAR). The types of
P W Schiller et al.
Journal of medicinal chemistry, 34(10), 3125-3132 (1991-10-01)
In an effort to determine the effect of side chain conformational restriction on opioid receptor selectivity, the cyclic phenylalanine analogues 2-aminoindan-2-carboxylic acid (Aic), 2-aminotetralin-2-carboxylic acid (Atc), and tetrahydroisoquinoline-3-carboxylic acid (Tic) were substituted for Phe in the potent cyclic opioid peptide
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