Welcome to LookChem.com Sign In|Join Free
  • or
1H-Benz[g]indole-2-carboxylic acid, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52280-53-2

Post Buying Request

52280-53-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

52280-53-2 Usage

Ethyl ester derivative

1H-Benz[g]indole-2-carboxylic acid, ethyl ester is derived from 1H-Benz[g]indole-2-carboxylic acid by attaching an ethyl group to the carboxylic acid functional group.

Indole compound

This chemical belongs to the class of compounds known as indoles, which are heterocyclic aromatic compounds.

Used as intermediate in synthesis

1H-Benz[g]indole-2-carboxylic acid, ethyl ester is often used as a starting material or intermediate in the synthesis of other pharmaceuticals and organic compounds.

Potential pharmacological properties

1H-Benz[g]indole-2-carboxylic acid, ethyl ester has been studied for its potential anti-inflammatory and anti-cancer effects.

Potential health hazards

This chemical may pose potential health hazards if not handled properly, and should be used with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 52280-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52280-53:
(7*5)+(6*2)+(5*2)+(4*8)+(3*0)+(2*5)+(1*3)=102
102 % 10 = 2
So 52280-53-2 is a valid CAS Registry Number.

52280-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1H-benzo[g]indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-Benz[g]indole-2-carboxylic acid,ethyl ester

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:52280-53-2 SDS

52280-53-2Downstream Products

52280-53-2Relevant academic research and scientific papers

Synthetic studies on indoles and related compounds. XXIX. Attempted syntheses of benz[f]indoles by cyclization reactions

Watanabe,Takahashi,Kamakura,Sakaguchi,Osaki,Toyama,Mizuma,Ueda,Murakami

, p. 3145 - 3152 (2007/10/02)

Syntheses of benz[f]indoles from 1,2-disubstituted naphthalene derivatives by means of cyclization reactions were attempted. The Fischer indolization of 1-methyl-(5a), 1-chloro-(5b), or 1-nitro-(5c)-2-naphthylhydrazones gave only benz[e]indole derivative or decomposed products, and the desired 9-substituted benz[f]indole (3) was not produced. On the other hand, the Fischer indolization of 2-methoxy-1-naphthylhydrazone (17) gave ethyl 5-chlorobenz[g]indole-2-carboxylate (19). The Hemetsberger reaction of 1-methoxy-2-naphthylazido acrylate (26a) gave an azirine (28a) and a nitrile (29a), whereas the same reaction of 1-chloro-2-naphthylazido acrylate (26b) gave the desired 4-chlorobenz[f]indole in a poor yield together with large amounts of by-products, the azirine (28b), the nitrile (29b) and the benz[g]indole (20). These results show that cyclization reactions of a 2-substituent toward the 3-position in naphthalene derivative are not suitable for preparing benz[f]indoles.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 52280-53-2