What is the 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE?

5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE is , while it's Molecular Formula is C10H13 N O. Used in Pharmaceutical Research: DOI is utilized as a research chemical for studying the 5-HT2A receptor's role in various psychological and neurological processes. Its agonistic action on this receptor provides insights into the mechanisms of hallucinations and other perceptual alterations. Used in Therapeutic Applications: In the field of medicine, DOI is considered for its potential therapeutic use as a treatment for mood and anxiety disorders. Its ability to interact with the 5-HT2A receptor suggests it may have efficacy in modulating these conditions, although further research is necessary to substantiate these claims. Used in Neurochemical Studies: DOI is employed in neurochemical research to explore the neurochemistry of consciousness and altered states of consciousness. Its effects on perception and cognition make it a valuable tool for understanding the underlying biochemical processes. Used in Drug Abuse Prevention and Education: Awareness of DOI's recreational use and its potential for abuse is crucial for drug abuse prevention and education efforts. Understanding the risks and adverse effects associated with its use can inform strategies to mitigate harm and promote responsible practices.

What is the CAS number for 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE?

The CAS number of 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE is 73305-09-6.

What is 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE (73305-09-6) used for?

5-Methoxy-2,3-dihydro-1H-inden-2-amine, commonly referred to as DOI, is a psychoactive phenethylamine compound that functions as a potent and selective agonist for the 5-HT2A receptor. This property endows it with hallucinogenic effects, leading to a range of psychedelic experiences such as visual and auditory hallucinations, altered thought patterns, and changes in the perception of time and space. DOI has garnered interest for its potential therapeutic applications in the treatment of mood and anxiety disorders, as well as for its contribution to the understanding of the neurochemistry of consciousness and altered states of consciousness. However, concerns exist regarding its recreational use due to the potential for abuse and adverse psychological effects.

What is the 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE?

5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE is , while it's Molecular Formula is C10H13 N O. Used in Pharmaceutical Research: DOI is utilized as a research chemical for studying the 5-HT2A receptor's role in various psychological and neurological processes. Its agonistic action on this receptor provides insights into the mechanisms of hallucinations and other perceptual alterations. Used in Therapeutic Applications: In the field of medicine, DOI is considered for its potential therapeutic use as a treatment for mood and anxiety disorders. Its ability to interact with the 5-HT2A receptor suggests it may have efficacy in modulating these conditions, although further research is necessary to substantiate these claims. Used in Neurochemical Studies: DOI is employed in neurochemical research to explore the neurochemistry of consciousness and altered states of consciousness. Its effects on perception and cognition make it a valuable tool for understanding the underlying biochemical processes. Used in Drug Abuse Prevention and Education: Awareness of DOI's recreational use and its potential for abuse is crucial for drug abuse prevention and education efforts. Understanding the risks and adverse effects associated with its use can inform strategies to mitigate harm and promote responsible practices.

What is the CAS number for 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE?

The CAS number of 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE is 73305-09-6.

What is 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE (73305-09-6) used for?

5-Methoxy-2,3-dihydro-1H-inden-2-amine, commonly referred to as DOI, is a psychoactive phenethylamine compound that functions as a potent and selective agonist for the 5-HT2A receptor. This property endows it with hallucinogenic effects, leading to a range of psychedelic experiences such as visual and auditory hallucinations, altered thought patterns, and changes in the perception of time and space. DOI has garnered interest for its potential therapeutic applications in the treatment of mood and anxiety disorders, as well as for its contribution to the understanding of the neurochemistry of consciousness and altered states of consciousness. However, concerns exist regarding its recreational use due to the potential for abuse and adverse psychological effects.

Product classification

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73305-09-6

Product Name:5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE
Molecular Formula:C10H13 N O
Molecular Weight:163.219

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Product Details

Purity:99%

Chinese factory supply 5-METHOXY-2,3-DIHYDRO-1H-INDEN-2-AMINE 73305-09-6 in stock with high standard

Molecular Formula:C10H13 N O
Molecular Weight:163.219
Boiling Point:277.6±40.0 °C(Predicted)
PKA:9.33±0.20(Predicted)
PSA：35.25000
Density:1.087±0.06 g/cm3(Predicted)
LogP:1.82140

73305-09-6 Relevant articles

Synthesis and asymmetric resolution of a dopaminergic compound: 2-amino-5-methoxyindane

Akbaba, Yusuf,G?ksu, Süleyman,?ahin, Ertan,Kili?, Hamdullah,Se?en, Hasan

, p. 475 - 479 (2016)

The racemic synthesis and subsequent res...

INDOLE AHR INHIBITORS AND USES THEREOF

-

Paragraph 00953; 00955, (2018/11/22)

The present invention provides compounds...

Synthesis method of 2-aminoindane derivative and product of 2-aminoindane derivative

-

, (2017/02/24)

The invention provides a synthesis metho...

SUBSTITUTED FLUOROETHYL UREAS AS ALPHA 2 ADRENERGIC AGENTS

-

Page/Page column 26, (2008/12/04)

Therapeutic compounds, and methods, comp...

73305-09-6 Process route

: 7235-36-1
5-methoxy-indan-1,2-dione 2-oxime

: 73305-09-6
(±)-2-amino-5-methoxyindane

Conditions

Conditions	Yield
5-methoxy-indan-1,2-dione 2-oxime; With sulfuric acid; hydrogen; palladium 10% on activated carbon; In acetic acid; for 18h; under 3102.97 Torr; With sodium hydroxide; In water; at 0 ℃; pH=10;	37%
5-methoxy-indan-1,2-dione 2-oxime; With sulfuric acid; hydrogen; palladium 10% on activated carbon; In acetic acid; for 18h; under 3102.97 Torr; With sodium hydroxide; In water; at 0 ℃; pH=10;	37%
With sulfuric acid; hydrogen; acetic acid; palladium on activated charcoal; for 18h; under 3102.97 Torr;	33%
With sulfuric acid; hydrogen; palladium on activated charcoal; In acetic acid; for 7h; under 2585.74 Torr;
With sulfuric acid; hydrogen; 10percent Pd/C; In acetic acid; for 7h; under 2585.81 Torr;
With sulfuric acid; palladium-carbon; palladium(II) chloride; In acetic acid;
With sulfuric acid; palladium-carbon; palladium(II) chloride; In acetic acid;
5-methoxy-indan-1,2-dione 2-oxime; With sulfuric acid; hydrogen; acetic acid; palladium 10% on activated carbon; under 2585.81 Torr; With sodium hydroxide;

: 81593-54-6
5-(methyloxy)-2,3-dihydro-1H-inden-2-amine hydrochloride

: 73305-09-6
(±)-2-amino-5-methoxyindane

Conditions

Conditions	Yield
With sodium hydroxide; In methanol; water; at 0 - 25 ℃; for 3h;	95%

73305-09-6 Upstream products

24077-98-3
2-(hydroxyimino)-6-methoxy-2,3-dihydro-1H-inden-1-one
1071698-32-2
2-amino-6-methoxy-indan-1-ol; hydrochloride
7235-36-1
5-methoxy-indan-1,2-dione 2-oxime
5111-70-6
5-methoxy-1-indanone

73305-09-6 Downstream products

81593-54-6
5-(methyloxy)-2,3-dihydro-1H-inden-2-amine hydrochloride
685832-33-1
2-(5-methoxyindane-2-yl)isoindole-1,3,dione

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