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136468-19-4

5-METHOXY-6-METHYL-2-AMINOINDAN is a chemical compound belonging to the aminoindan class of molecules. It features an indan structure with a methoxy group at the 5th position and a methyl group at the 6th position. 5-METHOXY-6-METHYL-2-AMINOINDAN has been studied for its potential pharmaceutical properties, particularly for its activity in the central nervous system. Its structural similarity to other psychoactive compounds has also led to investigations into its potential use as a psychoactive drug. Furthermore, it may have applications in medicinal chemistry and drug design. However, more research is required to fully understand its potential uses and effects.

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  • 136468-19-4 Structure

  • Basic information

    1. Product Name: 5-METHOXY-6-METHYL-2-AMINOINDAN
    2. Synonyms: 6-methoxy-5-methyl-2,3-dihydro-1H-inden-2-amine;1H-Inden-2-amine, 2,3-dihydro-5-methoxy-6-methyl-, (+-)-;5-Methoxy-6-methyl-2-aminoindan;
    3. CAS NO:136468-19-4
    4. Molecular Formula: C11H15NO
    5. Molecular Weight: 177.2429
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136468-19-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 286.8°Cat760mmHg
    3. Flash Point: 129.3°C
    4. Appearance: /
    5. Density: 1.065g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. PKA: 9.34±0.20(Predicted)
    10. CAS DataBase Reference: 5-METHOXY-6-METHYL-2-AMINOINDAN(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-METHOXY-6-METHYL-2-AMINOINDAN(136468-19-4)
    12. EPA Substance Registry System: 5-METHOXY-6-METHYL-2-AMINOINDAN(136468-19-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136468-19-4(Hazardous Substances Data)

136468-19-4 Usage

Uses

Used in Pharmaceutical Applications:
5-METHOXY-6-METHYL-2-AMINOINDAN is used as a compound with potential pharmaceutical properties due to its activity in the central nervous system. Its investigation for psychoactive drug development is driven by its structural similarity to other psychoactive compounds.
Used in Medicinal Chemistry and Drug Design:
In the field of medicinal chemistry and drug design, 5-METHOXY-6-METHYL-2-AMINOINDAN is utilized for its potential to contribute to the development of new drugs and therapeutic agents. Its unique structure and properties make it a candidate for further exploration and research in creating novel pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 136468-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,6 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136468-19:
(8*1)+(7*3)+(6*6)+(5*4)+(4*6)+(3*8)+(2*1)+(1*9)=144
144 % 10 = 4
So 136468-19-4 is a valid CAS Registry Number.

136468-19-4Downstream Products

136468-19-4Relevant articles and documents

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

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Paragraph 0094, (2017/02/24)

The invention provides a synthesis method of a 2-aminoindane derivative. According to the method, 5,6disubstituted 1-indanone is used as a staring raw material; bromination reaction is firstly performed; then, Gabriel reaction is performed; next, hydrazine hydrate is added; hydrolysis reaction is performed, and meanwhile, hydrazone is generated; finally, strong alkali is added into a high-boiling-point solvent to perform heating hydrolysis; the target product of the 2-aminoindane derivative is prepared. The invention also provides the 2-aminoindane derivative prepared by the synthesis method. Compared with the synthesis method of the 2-aminoindane derivative in the prior art, the synthesis method provided by the invention has the advantages that the reaction raw materials are cheap; the reaction condition is mild; the reaction steps are simple; the operation is easy; the yield of the obtained product is higher; the synthesis method is suitable for industrial production. Therefore good application prospects and market potentials are realized.

Synthesis and pharmacological examination of 1-(3-methoxy-4-methylphenyl)-2-aminopropane and 5-methoxy-6-methyl-2-aminoindan: Similarities to 3,4-(methylenedioxy)methamphetamine (MDMA)

Johnson,Frescas,Oberlender,Nichols

, p. 1662 - 1668 (2007/10/02)

The racemate and the enantiomers of 1-(3-methoxy-4-methylphenyl)-2-aminopropane (6) and racemic 5-methoxy-6-methyl-2-aminoindan (11) were tested for stimulus generalization in the two-lever drug-discrimination paradigm. Both 6 and 11 were found to substit

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