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CAS

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2826-96-2

(3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL is a versatile organic compound featuring an indole ring with an attached aminoethyl and methyl group, along with two hydrochloride groups. It is commonly utilized as a reagent in organic synthesis and pharmaceutical research, with potential applications in the development of drugs and medicinal compounds due to its ability to modulate biological processes. The presence of the aminoethyl group suggests that it may have interactions with biological systems, particularly with receptors or enzymes. The 2HCL designation indicates that two hydrochloride groups are associated with the compound, which can impact its solubility and stability in aqueous solutions.

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  • 2826-96-2 Structure

  • Basic information

    1. Product Name: (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL
    2. Synonyms: (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL ;2-(1-Methyl-1H-indol-3-yl)-ethylamine dihydrochloride;(3-(2-aminoethyl)-1-methylindole)dihydrochloride;3-(2-AMinoethyl)-1-Methylindole HCl;2-(1-Methyl-1H-indol-3-yl)ethan-1-amine hydrochloride
    3. CAS NO:2826-96-2
    4. Molecular Formula: C11H14N2*ClH
    5. Molecular Weight: 247.16414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2826-96-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 389.6°C at 760 mmHg
    3. Flash Point: 189.4°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 1.88E-06mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL(2826-96-2)
    12. EPA Substance Registry System: (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL(2826-96-2)

  • 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: 2826-96-2(Hazardous Substances Data)

2826-96-2 Usage

Uses

Used in Pharmaceutical Research and Development:
(3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL is used as a reagent in pharmaceutical research and development for its potential to modulate biological processes. (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL's unique structure allows it to interact with receptors or enzymes, making it a promising candidate for the development of new drugs and medicinal compounds.
Used in Organic Synthesis:
In the field of organic synthesis, (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL is used as a versatile building block for the synthesis of more complex organic molecules. Its unique functional groups, including the aminoethyl and methyl groups, enable it to participate in various chemical reactions, facilitating the creation of novel compounds with specific properties and applications.
Used in Drug Delivery Systems:
(3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL can be employed in drug delivery systems to improve the solubility, stability, and bioavailability of pharmaceutical compounds. The presence of the two hydrochloride groups can enhance the compound's solubility in aqueous solutions, which is crucial for the development of effective drug formulations.
Used in Biochemical Research:
In biochemical research, (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL can be used as a tool compound to study the interactions between small molecules and biological targets, such as receptors or enzymes. Its unique structure and functional groups make it suitable for investigating the molecular mechanisms underlying various biological processes and diseases.
Overall, (3-(2-AMINOETHYL)-1-METHYLINDOLE) 2HCL is a valuable chemical with diverse applications in pharmaceutical research, organic synthesis, drug delivery systems, and biochemical research, owing to its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 2826-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2826-96:
(6*2)+(5*8)+(4*2)+(3*6)+(2*9)+(1*6)=102
102 % 10 = 2
So 2826-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2.2ClH/c1-13-8-9(6-7-12)10-4-2-3-5-11(10)13;;/h2-5,8H,6-7,12H2,1H3;2*1H

2826-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methylindol-3-yl)ethanamine,dihydrochloride

1.2 Other means of identification

Product number -
Other names 2-(1-methylindol-3-yl)ethanamine dihydrochloride

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:2826-96-2 SDS

2826-96-2Downstream Products

2826-96-2Relevant articles and documents

Relay Catalysis of Rh (II) and Cobaloxime: Stereoselective Synthesis of Spiroindanones from N-Sulfonyl-1,2,3-triazoles

Liu, Zhao,Du, Qiuchen,Zhai, Hongbin,Li, Yun

, p. 7514 - 7517 (2018)

A novel relay Rh (II)/cobaloxime (III) dual catalysis strategy has been developed for the stereoselective synthesis of indolyl spiroindanones from readily accessible N-sulfonyl-1,2,3-triazoles. This binary-catalyst system enables an aza-vinyl carbene init

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