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5H-chroMeno[2,3-b]pyridin-7-ylacetic acid is a complex chemical compound belonging to the chromenopyridine class, characterized by a pyridine ring fused to a chromene ring and featuring an acetic acid group. This carboxylic acid derivative may exhibit acidic properties and could interact with various molecular targets in biological systems, indicating potential for biological activities. Further research is essential to uncover its applications in pharmacology, medicine, and other relevant fields.

52549-07-2

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52549-07-2 Usage

Uses

Used in Pharmaceutical Industry:
5H-chroMeno[2,3-b]pyridin-7-ylacetic acid is used as a potential pharmaceutical agent for its possible biological activities. Given its complex molecular structure and the presence of a carboxylic acid group, it may interact with molecular targets in biological systems, warranting investigation into its efficacy in treating specific conditions or diseases.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5H-chroMeno[2,3-b]pyridin-7-ylacetic acid serves as a subject for research to explore its potential as a lead compound. Its unique structure and chemical properties could be harnessed to develop new drugs or therapeutic agents, pending further exploration of its pharmacological profile.
Used in Chemical Synthesis:
5H-chroMeno[2,3-b]pyridin-7-ylacetic acid is used as a building block or intermediate in the synthesis of more complex organic compounds. Its versatile structure allows for various chemical modifications, making it a valuable component in the creation of novel molecules with specific applications in different industries.
Note: The specific applications listed above are hypothetical and based on the general properties of the compound. Without specific data on its biological activities or uses, these applications are speculative and would require experimental validation.

Check Digit Verification of cas no

The CAS Registry Mumber 52549-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52549-07:
(7*5)+(6*2)+(5*5)+(4*4)+(3*9)+(2*0)+(1*7)=122
122 % 10 = 2
So 52549-07-2 is a valid CAS Registry Number.

52549-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5H-chromeno[2,3-b]pyridin-7-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:52549-07-2 SDS

52549-07-2Downstream Products

52549-07-2Relevant academic research and scientific papers

Substituted alkanoic acids and derivatives

-

, (2008/06/13)

Substituted alkanoic acids and derivatives thereof of the formula: SPC1 Wherein each of X1 and X2 is a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; each of R1 and R2 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; A is a carbonyl group, a methylene group or an alkylidene group having 2 to 4 carbon atoms; Y is --O--, --S-- or --N(R)-- [wherein R is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms]; Z is OH or Q--B--N(R3)(R4) [wherein Q is O (oxygen atom) or NH, B is an alkylene group having 1 to 4 carbon atoms and each of R3 and R4 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or R3 and R4 together with the adjacent nitrogen atom form a saturated heterocycle selected from the group consisting of pyrrolidine, piperidine, morpholine, piperazine and piperazine substituted by an alkyl group having 1 to 4 carbon atoms at the 4-position]; and ring P represents a pyridine or a pyridine N-oxide ring; and pharmaceutically acceptable salts thereof are useful as antirheumatics, analgesics, antipyretics and anti-inflammatory agents.

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