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2,3-Diphenyl-1H-indole-7-carboxylic acid is a chemical compound with the molecular formula C22H17NO2. It belongs to the class of indole carboxylic acids and is a white to off-white solid. 2,3-DIPHENYL-1H-INDOLE-7-CARBOXYLIC ACID is known for its unique molecular structure and properties, which make it a valuable candidate in various fields of research and development.

197313-74-9

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197313-74-9 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
2,3-Diphenyl-1H-indole-7-carboxylic acid is used as a key intermediate in the synthesis of potential pharmacological agents. Its chemical properties and structure contribute to the development of new drugs with therapeutic applications.
Used in Anticancer Applications:
In the field of oncology, 2,3-diphenyl-1H-indole-7-carboxylic acid is used as a potential anticancer agent. It has been studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for further research and development in cancer treatment.
Used in Antiviral Applications:
2,3-Diphenyl-1H-indole-7-carboxylic acid is also being explored for its potential as an antiviral agent. Its molecular properties may allow it to interfere with viral replication and infection, offering a new avenue for antiviral drug development.
Used in Anti-inflammatory and Analgesic Applications:
2,3-DIPHENYL-1H-INDOLE-7-CARBOXYLIC ACID is used in the development of anti-inflammatory and analgesic drugs. Its potential to reduce inflammation and alleviate pain makes it a valuable asset in the search for new treatments for conditions such as arthritis and other inflammatory diseases.
Used in Material Science and Organic Electronics:
2,3-Diphenyl-1H-indole-7-carboxylic acid is used in the development of new materials and organic electronic devices. Its unique molecular structure and properties lend themselves to applications in areas such as organic light-emitting diodes (OLEDs), organic solar cells, and other advanced electronic technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 197313-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,3,1 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 197313-74:
(8*1)+(7*9)+(6*7)+(5*3)+(4*1)+(3*3)+(2*7)+(1*4)=159
159 % 10 = 9
So 197313-74-9 is a valid CAS Registry Number.

197313-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Diphenyl-1H-indole-7-carboxylic acid

1.2 Other means of identification

Product number -
Other names HMS2757D14

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:197313-74-9 SDS

197313-74-9Relevant academic research and scientific papers

NOVEL INDOLE DERIVATES AS FABP-4 INHIBITORS

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Page 43-44, (2010/02/07)

The present invention relates to novel compounds (I) wherein R0, R1, R2, R3, R4, R5, R6, R7, R8, A, B, n, X, and Y are as defined in the description and claims; and also to pharmaceutical compositions comprising the compounds, as well as to the use of the compounds in medicine and for the preparation of a medicament, which acts on the fatty acid binding protein FABP-4. The present invention relates to novel compounds (I) wherein R0, R1, R2, R3, R4, R5, R6, R7, R8, A, B, n, X, and Y are as defined in the description and claims; and also to pharmaceutical compositions comprising the compounds, as well as to the use of the compounds in medicine and for the preparation of a medicament, which acts on the fatty acid binding protein FABP-4.

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