CAS 2338-18-3

2-Aminoindan hydrochloride

Description:

2-Aminoindan hydrochloride is a chemical compound characterized by its structure, which features an indan ring system with an amino group at the 2-position. This compound is typically encountered as a hydrochloride salt, enhancing its solubility in water and making it suitable for various applications in research and pharmaceuticals. It is known for its potential use in the synthesis of other organic compounds and may exhibit biological activity, including effects on the central nervous system. The presence of the amino group allows for various chemical reactions, such as acylation or alkylation, facilitating the development of derivatives with tailored properties. Additionally, 2-aminoindan hydrochloride is often studied for its role in medicinal chemistry, particularly in the context of developing new therapeutic agents. As with many chemical substances, safety precautions should be observed when handling it, as it may pose health risks if ingested or inhaled. Proper storage conditions are also essential to maintain its stability and efficacy.

Formula: C₉H₁₂ClN

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

InChI key: InChIKey=XEHNLVMHWYPNEQ-UHFFFAOYSA-N

SMILES: NC1CC=2C(C1)=CC=CC2.Cl

Synonyms:

• (2,3-Dihydro-1H-inden-2-yl)amine hydrochloride
• 1H-Inden-2-amine, 2,3-dihydro-, hydrochloride
• 1H-Inden-2-amine, 2,3-dihydro-, hydrochloride (1:1)
• 1H-Inden-2-amine, 2,3-dihydro-, hydrochloride (9CI)
• 2,3-Dihydro-1H-inden-2-amine hydrochloride
• 2,3-Dihydro-1H-inden-2-aminium chloride
• 2,3-dihydro-1H-inden-2-amine
• 2,3-dihydro-1H-inden-2-amine hydrochloride (1:1)
• 2-AMINOINDANE HCl
• 2-Amino-2,3-dihydro-1H-indene hydrochloride
• 2-Aminoindan HCl
• 2-Aminoindan monohydrochloride
• 2-Aminoindane hydrochloride
• 2-Indanamine, hydrochloride
• 2-Indanylamine hydrochloride
• Indan-2-ylamine hydrochloride
• Indan-2-ylammonium chloride
• Nsc 48663
• Nsc 78117
• Su 8629 hydrochloride
• 2-Aminoindan hydrochloride
• 2-indanylaminehydrochloride
• 2,3-dihydro-1h-inden-2-aminehydrochloride
• TIMTEC-BB SBB003858
• 2,3-DIHYDRO-1H-INDEN-2-AMINE HCL
• 2-INDANAMINE HCL
• 2-Aminoindane hydrochloride 98%

2-Aminoindane hydrochloride, 98%

CAS: 2338-18-3

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₉H₁₁ClN

Purity: 98%

Color and Shape: White to cream to yellow, Crystals or powder or crystalline powder

Molecular weight: 168.64

Ref: 02-L14083

2-Aminoindane Hydrochloride (2-AI HCl) 1.0 mg/ml in Methanol (as free base)

Controlled Product

CAS: 2338-18-3

Color and Shape: Single Solution

Ref: 61-AMP1275.50-01

2-Aminoindane Hydrochloride (2-AI HCl)

Controlled Product

CAS: 2338-18-3

Color and Shape: Neat

Ref: 61-FOR1275.50

2-Aminoindan hydrochloride

CAS: 2338-18-3

Formula: C₉H₁₁N·HCl

Purity: ≥ 98.0%

Color and Shape: White to off-white powder

Molecular weight: 169.66

Ref: 7W-GK6790

2-Aminoindane hydrochloride

CAS: 2338-18-3

2-Aminoindane hydrochloride

Formula: C₉H₁₁N·ClH

Purity: 98%

Color and Shape: off white solid

Molecular weight: 169.65g/mol

Ref: 54-OR30439

2-Aminoindan Hydrochloride

Controlled Product

CAS: 2338-18-3

Applications Hydrochloride salt of 2-Aminoindan is an analgesic with sympathomimetic activity. 2-Aminoindan is an inhibitor norepinephrine methyltransferase.
References Burn, P. et al.: J. Pharm. Pharmacol., 28, 80P (1976); Fuller, R. et al.: Biochem. Pharmacol., 26, 446 (1977);

Formula: C₉H₁₁N·ClH

Color and Shape: Neat

Molecular weight: 169.65

Ref: TR-A611825

2-Aminoindane HCl

Controlled Product

CAS: 2338-18-3

2-Aminoindane HCl is a betalamic acid derivative that inhibits the activity of the dopamine receptor. It has been shown to inhibit the binding of dopamine in both rat and human liver, as well as in a model system. 2-Aminoindane HCl is formed by intramolecular hydrogenation of betalamic acid and hydrolysis of the resulting 2-aminoindane acetic acid chloride. The carbonic ester group on the indane ring forms an alkoxy radical with hydrogen chloride in water, which then reacts with a hydroxy group on the indane ring to form 2-aminoindane HCl. This process can be modeled using molecular modeling techniques.

Purity: Min. 95%

Molecular weight: 169.65 g/mol

Ref: 3D-FA00485

Indacaterol Impurity 11

CAS: 2338-18-3

Formula: C₉H₁₁NHCl

Molecular weight: 133.2 : 36.5

Ref: ST-EA-CP-I13018

1H-Inden-2-amine, 2,3-dihydro-, hydrochloride (1:1)

CAS: 2338-18-3

Formula: C₉H₁₂ClN

Color and Shape: Solid

Molecular weight: 169.6513

Ref: IN-DA002N1B