Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Methyl 2-(1H-indol-2-yl)acetate is a chemical compound with the molecular formula C12H13NO2. It is an indole derivative, which is a common structural motif found in many natural products and pharmaceuticals. methyl 2-(1H-indol-2-yl)acetate is known for its potential applications in various fields due to its unique chemical properties.

21422-40-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 21422-40-2 Structure
  • Basic information

    1. Product Name: methyl 2-(1H-indol-2-yl)acetate
    2. Synonyms: methyl 2-(1H-indol-2-yl)acetate;methyl indole-2-acetate
    3. CAS NO:21422-40-2
    4. Molecular Formula: C11H11NO2
    5. Molecular Weight: 189.21054
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21422-40-2.mol
  • Chemical Properties

    1. Melting Point: 68-69 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3))
    2. Boiling Point: 341.8±17.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.223±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 16.68±0.30(Predicted)
    10. CAS DataBase Reference: methyl 2-(1H-indol-2-yl)acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 2-(1H-indol-2-yl)acetate(21422-40-2)
    12. EPA Substance Registry System: methyl 2-(1H-indol-2-yl)acetate(21422-40-2)
  • 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: 21422-40-2(Hazardous Substances Data)

21422-40-2 Usage

Uses

Used in Organic Synthesis:
Methyl 2-(1H-indol-2-yl)acetate is used as a building block in organic synthesis for the preparation of various indole-based compounds. Its versatile structure allows for the creation of a wide range of chemical entities, making it a valuable component in the development of new molecules.
Used in Pharmaceutical Industry:
As a starting material, methyl 2-(1H-indol-2-yl)acetate is utilized in the synthesis of pharmaceuticals. Its presence in the molecular structure of numerous bioactive compounds makes it an essential precursor in the development of new drugs with potential therapeutic applications.
Used in Agrochemicals:
Methyl 2-(1H-indol-2-yl)acetate also serves as a starting material in the synthesis of agrochemicals. Its role in creating compounds with pesticidal or herbicidal properties contributes to the advancement of agricultural solutions to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
Due to its biological activities, methyl 2-(1H-indol-2-yl)acetate is an important target in medicinal chemistry research. Scientists explore its potential to contribute to the discovery of new therapeutic agents, particularly those that interact with biological systems in meaningful ways.

Check Digit Verification of cas no

The CAS Registry Mumber 21422-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,2 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21422-40:
(7*2)+(6*1)+(5*4)+(4*2)+(3*2)+(2*4)+(1*0)=62
62 % 10 = 2
So 21422-40-2 is a valid CAS Registry Number.

21422-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(1H-indol-2-yl)acetate

1.2 Other means of identification

Product number -
Other names methyl indole-2-acetate

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:21422-40-2 SDS

21422-40-2Relevant articles and documents

Nucleophilic Additions to Pyridium Salts. Reduction of the Intermediate Dihydropyridines

Lavilla, Rodolfo,Gotsens, Teresa,Gullon, Francisco,Bosch, Joan

, p. 5233 - 5244 (1994)

Reduction of indolyldihydropyridines 4 and 5 satisfactorily gave the corresponding tetrahydropyridines 6 and 7.A similar reduction of 4-(2-indolylmethyl)-1,4-dihydropyridines 3 was inefficient.In contrast, dihydropyridine 19 was reduced to 23 and then cyclized to pentacycle 24.Direct cyclization of 19 resulted in the formation of imide 21.

Synthesis and in vitro antitumor activity of novel 2-alkyl-5- methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazol-2-ium and 2-alkylellipticin-2-ium chloride derivatives

Mori, Ryota,Kato, Asako,Komenoi, Kousuke,Kurasaki, Haruaki,Iijima, Touru,Kawagoshi, Masashi,Kiran,Takeda, Sho,Sakai, Norio,Konakahara, Takeo

, p. 16 - 35 (2014/06/09)

Twenty-one types of novel ellipticine derivatives and pyridocarbazoles (5-methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazoles) with a nitrosourea moiety, linked by an oxydiethylene unit at the 2 position, were synthesized, and their cytotoxicity against HeLa S-3 cells was evaluated. Some of these new compounds exhibited potent antitumor activity by comparison with that of ellipticine.

Synthesis of the Benzazepin-4-one Ring System via Dipolar Cycloaddition of N-Phenylnitrones with Activated Allenes

Padwa, Albert,Kline, Donald N.,Norman, Bryan H.

, p. 810 - 817 (2007/10/02)

The 1,3-dipolar cycloaddition of N-phenyl-C-phenylnitrone with several allenes containing electron-withdrawing groups has been investigated.The cycloaddition proceeds in good yields to give a substituted benzazepin-4-one.The structure of the cycloadduct w

SYNTHESIS OF ELLIPTICINE

Weller, Dwight D.,Ford, Douglas W.

, p. 2105 - 2108 (2007/10/02)

The 6H-pyridocarbazole system is efficiently synthesized by intramolecular attack of an ester enolate on an unactivated pyridinium salt.

Etude spectroscopique (IR, RMN1H, masse) comparee des acides indolyl-1 acetique (AIA-1) indolyl-2 acetique (AIA-2) et indolyl-3 acetique (AIA-3) et de leurs esters methyliques (masse)

Vebrel, Joel,Laude, Bernard,Seguin, Alain,Dubouchet, Jacques

, p. 887 - 894 (2007/10/02)

Spectroscopic study (i.r., PMR) of 1-indolyl, 2-indolyl and 3-indolyl acetic acids points out structural differences.Conventional mass spectra of the three acids or their methyl esters are very similar.Use of the MIKE and CID-MIKE techniques on the molecular ion allows an easy discrimination of each methylic ester of the three acids.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 21422-40-2