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132980-16-6 Usage

Description

5-Methoxy-6-methyl-2-aminoindan, also known as 5-MMAI, is a chemical compound that belongs to the class of tryptamines, a group of substances with a common chemical backbone. It exhibits structural similarities to hallucinogenic, psychedelic drugs like LSD and DMT, and designer drugs like MDMA. However, the exact physiological and toxicological properties of this substance are not well known due to little to no recorded history of human usage.

Uses

Used in Scientific Research:
5-Methoxy-6-methyl-2-aminoindan is used as a research chemical for studying its potential psychoactive effects and structural relationship to other tryptamines. Given its similarities to hallucinogenic and psychedelic drugs, it may provide insights into the mechanisms of action and potential therapeutic applications of these substances.
Used in Analytical Chemistry:
5-Methoxy-6-methyl-2-aminoindan is used as a reference compound in analytical chemistry for the development and validation of analytical methods, such as chromatography and mass spectrometry, for the detection and quantification of tryptamines and related compounds.
Used in Forensic Science:
5-Methoxy-6-methyl-2-aminoindan is used as a reference substance in forensic science for the identification and analysis of tryptamines and related compounds in biological samples, such as blood, urine, and tissue, to aid in the investigation of drug-related crimes and toxicological cases.
Used in Drug Development:
Although not intended for human consumption, 5-Methoxy-6-methyl-2-aminoindan may be used as a lead compound in drug development for the synthesis of new psychoactive substances with potential therapeutic applications. Its structural relationship to known psychoactive drugs may provide a basis for the design of novel compounds with improved safety and efficacy profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 132980-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,8 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132980-16:
(8*1)+(7*3)+(6*2)+(5*9)+(4*8)+(3*0)+(2*1)+(1*6)=126
126 % 10 = 6
So 132980-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c1-7-3-8-4-10(12)5-9(8)6-11(7)13-2/h3,6,10H,4-5,12H2,1-2H3

132980-16-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methoxy-6-methyl-2,3-dihydro-1H-inden-2-amine

1.2 Other means of identification

Product number -
Other names 5-methoxy-6-methyl-2,3-dihydro-1H-inden-2-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132980-16-6 SDS

132980-16-6Downstream Products

132980-16-6Relevant 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.

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