CAS 2975-41-9

2-Aminoindane

Description:

2-Aminoindane is an organic compound characterized by its bicyclic structure, which consists of an indane framework with an amino group (-NH2) attached to the second carbon of the indane ring. This compound is a derivative of indane, a bicyclic hydrocarbon, and is known for its potential applications in medicinal chemistry and as a building block in organic synthesis. 2-Aminoindane is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents and exhibits basic properties due to the presence of the amino group. The compound has garnered interest for its potential psychoactive effects and has been studied for its interactions with neurotransmitter systems. Additionally, 2-aminoindane can undergo various chemical reactions, including alkylation and acylation, making it a versatile intermediate in the synthesis of more complex molecules. Safety data indicates that, like many amines, it should be handled with care due to potential irritant properties.

Formula: C₉H₁₁N

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

InChI key: InChIKey=LMHHFZAXSANGGM-UHFFFAOYSA-N

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

Synonyms:

• (2,3-Dihydro-1H-inden-2-yl)amine
• 1H-Inden-2-amine, 2,3-dihydro-
• 2,3-Dihydro-1H-inden-2-amine
• 2-Amino-2,3-dihydro-1H-indene
• 2-AminoIndane
• 2-Aminoindan
• 2-Indanamine
• 2-Indanylamine
• Su 8629

2-Aminoindan

CAS: 2975-41-9

Formula: C₉H₁₁N

Purity: >99.0%(GC)(T)

Color and Shape: Colorless to Purple to Brown clear liquid

Molecular weight: 133.19

Ref: 3B-A1320

2-Aminoindan

Controlled Product

CAS: 2975-41-9

2-Aminoindan is a compound that has inhibitory properties against the human liver enzyme dopamine β-hydroxylase. It binds to the active site of the enzyme and inhibits its activity, which decreases the production of dopamine and other monoamines in the body. 2-Aminoindan has been shown to be effective in animal models of Parkinson's disease by reducing oxidative stress and restoring dopamine levels. The drug also has a chemical diversity, with many different possible structures for medicinal use. 2-Aminoindan has been shown to inhibit the formation of carbonic acid, which is used by mammalian tissue as a buffer for pH regulation. This property may account for its inhibitory effect on carbonic anhydrase II (CAII), an enzyme involved in tissue respiration and acid-base balance. 2-Aminoindan has also been shown to have inhibitory effects on two bacterial enzymes: ddpP and ddpD, which are involved

Formula: C₉H₁₁N

Purity: Min. 95%

Molecular weight: 133.19 g/mol

Ref: 3D-FA17764

1H-Inden-2-amine, 2,3-dihydro-

CAS: 2975-41-9

Formula: C₉H₁₁N

Molecular weight: 133.1903

Ref: IN-DA002ZAK