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2-(2-cyano-4-Methoxyphenyl)acetic acid is a chemical compound with the molecular formula C11H9NO3. It is a derivative of acetic acid, featuring a cyano and a methoxy group attached to a benzene ring. 2-(2-cyano-4-Methoxyphenyl)acetic acid is known for its unique chemical structure and reactivity, which makes it a valuable asset in chemical and pharmaceutical research.

52786-67-1

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52786-67-1 Usage

Uses

Used in Pharmaceutical Research:
2-(2-cyano-4-Methoxyphenyl)acetic acid is used as a research compound for its potential to modulate biological processes. Its unique structure allows it to interact with various biological targets, making it a promising candidate for drug development.
Used in Drug Development:
In the pharmaceutical industry, 2-(2-cyano-4-Methoxyphenyl)acetic acid is utilized as a lead compound for the development of new drugs. Its ability to modulate biological processes suggests potential therapeutic applications in treating various diseases and conditions.
Used in Antibacterial Applications:
2-(2-cyano-4-Methoxyphenyl)acetic acid is studied for its potential antibacterial properties. It may be used as an active ingredient in antimicrobial agents to combat bacterial infections.
Used in Anti-inflammatory Applications:
2-(2-cyano-4-Methoxyphenyl)acetic acid has also been investigated for its potential anti-inflammatory effects. It could be used as an anti-inflammatory agent to alleviate inflammation and related symptoms in various conditions.
Used in Organic Synthesis:
Due to its unique chemical structure and reactivity, 2-(2-cyano-4-Methoxyphenyl)acetic acid may have uses in the synthesis of other organic compounds. It can serve as a building block or intermediate in the production of various organic molecules for different applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 52786-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,8 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52786-67:
(7*5)+(6*2)+(5*7)+(4*8)+(3*6)+(2*6)+(1*7)=151
151 % 10 = 1
So 52786-67-1 is a valid CAS Registry Number.

52786-67-1SDS

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 (2-cyano-4-methoxyphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-Cyano-4-methoxyphenyl)acetic 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:52786-67-1 SDS

52786-67-1Relevant academic research and scientific papers

Evaluation and synthesis of polar aryl- and heteroaryl spiroazetidine-piperidine acetamides as ghrelin inverse agonists

Orr, Suvi T. M.,Beveridge, Ramsay,Bhattacharya, Samit K.,Cameron, Kimberly O.,Coffey, Steven,Fernando, Dilinie,Hepworth, David,Jackson, Margaret V.,Khot, Vishal,Kosa, Rachel,Lapham, Kimberly,Loria, Paula M.,McClure, Kim F.,Patel, Jigna,Rose, Colin,Saenz, James,Stock, Ingrid A.,Storer, Gregory,Von Volkenburg, Maria,Vrieze, Derek,Wang, Guoqiang,Xiao, Jun,Zhang, Yingxin

supporting information, p. 156 - 161 (2015/03/04)

Several polar heteroaromatic acetic acids and their piperidine amides were synthesized and evaluated as ghrelin or type 1a growth hormone secretagogue receptor (GHS-R1a) inverse agonists. Efforts to improve pharmacokinetic and safety profile was achieved

2,3-DIHYDRO-1H-INDEN-1-YL-2,7-DIAZASPIRO[3.5] NONANE DERIVATIVES

-

Page/Page column 31, (2011/10/10)

The present invention provides a compound of Formula (I) or a pharmaceutically salt thereof wherein R1, R2, Ra, L, Z, Z1 and Z2 are as defined herein, that act as Ghrelin antagonists or inverse agonists; pharmaceutical compositions thereof; and methods of treating diseases, disorders, or conditions mediated by the antagonism of the Ghrelin receptor.

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