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A59522

2-Aminoindan hydrochloride

Name: 2-Aminoindan hydrochloride
Brand: ALDRICH

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

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891039

EC Number:

219-048-0

Beilstein/REAXYS Number:

3913700

MDL number:

MFCD00012549

Assay:

98%

Form:

crystals

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Properties

Quality Level

100

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

Description

Application

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

pictograms

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

监管及禁止进口产品

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Forensic electrochemistry: indirect electrochemical sensing of the components of the new psychoactive substance "Synthacaine".

Loanda R Cumba et al.

The Analyst, 140(16), 5536-5545 (2015-06-24)

"Synthacaine" is a New Psychoactive Substance which is, due to its inherent psychoactive properties, reported to imitate the effects of cocaine and is therefore consequently branded as "legal cocaine". The only analytical approach reported to date for the sensing of

Conformational analysis of 2-aminoindans and 2-(aminomethyl)indans in relation to their central dopaminergic effects and a dynamic dopamine receptor concept.

H Wikström et al.

Journal of medicinal chemistry, 30(7), 1115-1120 (1987-07-01)

Conformational analyses on differently substituted 2-aminoindans of significant pharmacological interest were carried out by the molecular mechanics method (MM2). An X-ray structure of (R)-4-methoxy-2-aminoindan has shown the ammonium nitrogen [-)-D-tartaric acid salt) in an axial position. From comparison with other

Structure-activity relationships of 2-aminotetralins and 2-aminoindanes: inhibitory neuroeffector mechanisms in isolated guinea-pig ilea.

S P Arnerić et al.

Archives internationales de pharmacodynamie et de therapie, 258(1), 84-99 (1982-07-01)

The ability of 2-aminotetralins (2-ATs), 2-aminoindanes (2-AIs), morphine (M) and clonidine (CLON) to alter neuroeffector transmission was studied on field-stimulated (FS) guinea-pig ilea (GPI). The activity of these compounds to inhibit K+, histamine (H), actylcholine (ACh), nicotine (Nic) and serotonin

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Global Trade Item Number

SKU	GTIN
A59522-25G	04061832103020
A59522-5G	04061832089041