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2-(1-Methyl-3-indolyl)-2-phenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125879-68-7 Structure
  • Basic information

    1. Product Name: 2-(1-Methyl-3-indolyl)-2-phenylethanol
    2. Synonyms: 2-(1-Methyl-3-indolyl)-2-phenylethanol
    3. CAS NO:125879-68-7
    4. Molecular Formula: C17H17NO
    5. Molecular Weight: 251
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125879-68-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(1-Methyl-3-indolyl)-2-phenylethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Methyl-3-indolyl)-2-phenylethanol(125879-68-7)
    11. EPA Substance Registry System: 2-(1-Methyl-3-indolyl)-2-phenylethanol(125879-68-7)
  • 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: 125879-68-7(Hazardous Substances Data)

125879-68-7 Usage

Biological activity

Potential antioxidant, anti-inflammatory, and anti-tumor properties These properties suggest that the compound may help protect cells from damage, reduce inflammation, and inhibit the growth of tumors.

Natural sources

Found in plants and microorganisms This indicates that 2-(1-Methyl-3-indolyl)-2-phenylethanol is present in various natural environments, which could contribute to its potential health benefits.

Pharmaceutical applications

Potential use in pharmaceuticals The compound's biological activity makes it a candidate for the development of new drugs to treat various health conditions.

Natural food additive

Potential use as a natural food additive Due to its potential health benefits, 2-(1-Methyl-3-indolyl)-2-phenylethanol could be used as a supplement or additive in food products.

Immune response regulation

Potential role in regulating immune response This suggests that the compound may help modulate the immune system, which could be beneficial in treating immune-related disorders.

Neuroprotective agent

Potential as a neuroprotective agent The compound may have the ability to protect neurons from damage, which could be useful in treating neurological disorders.

Unique structure

Interesting target for further research and development The compound's structure makes it a promising candidate for further study in various fields, including pharmaceuticals, food additives, and potential health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 125879-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,7 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125879-68:
(8*1)+(7*2)+(6*5)+(5*8)+(4*7)+(3*9)+(2*6)+(1*8)=167
167 % 10 = 7
So 125879-68-7 is a valid CAS Registry Number.

125879-68-7Downstream Products

125879-68-7Relevant articles and documents

A simple, highly regioselective and efficient reaction of indole with epoxides under solvent-free conditions

Azizi, Najmedin,Mehrazma, Shokopheh,Saidi, Mohammad R.

, p. 800 - 803 (2006)

Lithium perchlorate has been found to be an inexpensive and efficient catalyst for the ring opening of epoxides by indole and N-methylindole, which provides an environmentally friendly method for the synthesis of substituted indoles. A complete regioselec

Iron-containing ionic liquid as an efficient and recyclable catalyst for the synthesis of C3-substituted indole derivatives

Gu, Ying-Chun,Hu, Ren-Ming,Li, Ming-Ming,Xu, Da-Zhen

, (2019)

A facile and efficient protocol for the synthesis of C3-substituted indole derivatives has been developed under mild condition. The iron-containing ionic liquid, 1-(2-hydroxyethyl)-1,4-diazabicyclo[2.2.2] octanylium tetrachloroferrate ([Dabco-C2/sub

Friedel-Crafts alkylation of indoles with epoxides catalyzed by nanocrystalline titanium(IV) oxide

Kantam, M. Lakshmi,Laha, Soumi,Yadav, Jagjit,Sreedhar

, p. 6213 - 6216 (2006)

Friedel-Crafts alkylation of indoles with epoxides to afford 3-alkyl indole derivatives at room temperature with moderate to good yields and high regioselectivity using nanocrystalline titanium(IV) oxide catalyst is described.

A facile synthesis of alkylated nitrogen heterocycles catalysed by 3D mesoporous aluminosilicates with cage type pores in aqueous medium

Chakravarti, Rajashree,Kalita, Pranjal,Selvan, S. Tamil,Oveisi, Hamid,Balasubramanian,Kantam, M. Lakshmi,Vinu, Ajayan

, p. 49 - 53 (2010)

Friedel-Crafts alkylation of nitrogen heterocycles such as indoles and pyrroles with epoxides has been efficiently carried out using cage-type mesoporous aluminosilicates as recyclable catalysts in water under environmentally benign and mild conditions.

MIL-101(Fe) as an active heterogeneous solid acid catalyst for the regioselective ring opening of epoxides by indoles

Nagarjun, Nagarathinam,Concepcion, Patricia,Dhakshinamoorthy, Amarajothi

, (2019/12/09)

Ring opening of an epoxide by a nucleophile is considered as one of the viable strategies to prepare biologically active molecules using homogeneous or heterogeneous Lewis acid catalysts. Very often, the ring opening of epoxide was performed with oxygen,

Regio- and enantioselective Friedel-Crafts reactions of indoles to epoxides catalyzed by graphene oxide: A green approach

Acocella, Maria Rosaria,Mauro, Marco,Guerra, Gaetano

, p. 3279 - 3283 (2015/02/03)

Graphene oxide efficiently promotes high regio- and enantioselective ring opening reactions of aromatic epoxides by indoles addition, in solvent- and metal-free conditions. The Friedel-Crafts products were obtained with enantioselectivity up to 99% ee. Th

Magnetic nano Fe3O4 and CuFe2O4 as heterogeneous catalysts: A green method for the stereo- and regioselective reactions of epoxides with indoles/pyrroles

Parella, Ramarao,Naveen,Babu, Srinivasarao Arulananda

, p. 118 - 121 (2013/01/15)

In this paper, we report a new solvent-free catalytic method using the magnetic nano Fe3O4 and CuFe2O4 as competent heterogeneous catalysts for the stereo- and regioselective reactions of epoxides with indoles/p

Friedel-Crafts Alkylation of Nitrogen Heterocycles Using [Bmim][OTf] as a Catalyst and Reaction Medium

Kantam, M. Lakshmi,Chakravarti, Rajashree,Sreedhar,Bhargava, Suresh

experimental part, p. 1449 - 1454 (2009/04/07)

Friedel-Crafts alkylation of nitrogen heterocycles, such as indoles and pyrroles, can be carried out in ionic liquids under mild conditions to afford the corresponding alkylated product in moderate to good yields.

High-pressure organic chemistry. 19. High-pressure-promoted, silica gel-catalyzed reaction of epoxides with nitrogen heterocycles

Kotsuki, Hiyoshizo,Hayashida, Katsunori,Shimanouchi, Tomoyasu,Nishizawa, Hitoshi

, p. 984 - 990 (2007/10/03)

The reaction of epoxides with nitrogen heterocycles such as indoles, pyrroles, imidazoles, and pyrazoles was studied under both high-pressure and silica gel-catalyzed conditions. Whereas it has been reported that the treatment of indole with styrene oxide

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