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5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is a chemical compound characterized by the molecular formula C20H15NO3. It is a carboxylic acid derivative of the indole structure, featuring a benzyl ether group at the 5-position. 5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is notable for its potential applications in organic synthesis and medicinal chemistry due to the biological activities associated with indole derivatives, such as antibacterial, antifungal, and anticancer properties. The carboxylic acid group present in its structure further enhances its value as an intermediate in the synthesis of pharmaceuticals and bioactive compounds. Its distinctive structural features and potential reactivity also make it a compelling subject for ongoing research and development within the realm of organic chemistry.

24370-73-8

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24370-73-8 Usage

Uses

Used in Organic Synthesis:
5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the creation of a wide range of compounds with potential applications in different fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is utilized as a precursor for the development of new pharmaceuticals. Its biological activities, such as antibacterial, antifungal, and anticancer properties, make it a promising candidate for the treatment of various diseases and conditions.
Used in Pharmaceutical Industry:
5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is used as a building block in the pharmaceutical industry for the synthesis of drugs with potential therapeutic effects. The presence of the carboxylic acid group allows for easy derivatization and modification, enabling the design of novel drug molecules with improved pharmacological properties.
Used in Research and Development:
5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is employed as a subject of research and development in the field of organic chemistry. Its unique structure and potential reactivity offer opportunities for the exploration of new chemical reactions and the discovery of innovative synthetic pathways.
Used in Bioactive Compounds Synthesis:
In the synthesis of bioactive compounds, 5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID is used as a valuable intermediate. Its incorporation into the molecular structures of these compounds can enhance their biological activities, leading to the development of new agents with potential applications in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 24370-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24370-73:
(7*2)+(6*4)+(5*3)+(4*7)+(3*0)+(2*7)+(1*3)=98
98 % 10 = 8
So 24370-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO3/c18-16(19)14-9-17-15-7-6-12(8-13(14)15)20-10-11-4-2-1-3-5-11/h1-9,17H,10H2,(H,18,19)

24370-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylmethoxy-1H-indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-BENZYLOXY-1H-INDOLE-3-CARBOXYLIC ACID

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:24370-73-8 SDS

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