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4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is a pyrrole derivative characterized by a molecular formula of C11H13NO3. It features an acetyl group and two methyl substituents, which contribute to its unique chemical properties. 4-ACETYL-3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID has garnered attention in the fields of pharmaceuticals and organic synthesis due to its potential applications as a building block for the synthesis of heterocyclic compounds and pharmaceutical intermediates. Moreover, it has been investigated for its anti-inflammatory and anti-cancer properties, positioning it as a promising candidate in medicinal chemistry. However, further research is essential to fully explore and understand its potential uses and applications.

2386-28-9

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2386-28-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is used as a building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid serves as a key intermediate for the preparation of complex organic molecules. Its reactivity and versatility allow for the formation of diverse chemical entities, contributing to the advancement of organic chemistry.
Used in Medicinal Chemistry:
4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is used as a subject of interest in medicinal chemistry due to its potential anti-inflammatory and anti-cancer properties. Its ability to modulate biological pathways and exhibit therapeutic effects makes it a promising candidate for the development of novel pharmaceutical agents.
Used in Research and Development:
In the realm of research and development, 4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is utilized as a test compound to explore its potential applications and understand its mechanisms of action. Further studies are necessary to fully elucidate its capabilities and optimize its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2386-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2386-28:
(6*2)+(5*3)+(4*8)+(3*6)+(2*2)+(1*8)=89
89 % 10 = 9
So 2386-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-4-7(6(3)11)5(2)10-8(4)9(12)13/h10H,1-3H3,(H,12,13)/p-1

2386-28-9 Well-known Company Product Price

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  • Aldrich

  • (A15002)  4-Acetyl-3,5-dimethyl-2-pyrrolecarboxylicacid  95%

  • 2386-28-9

  • A15002-10G

  • 363.87CNY

  • Detail
  • Aldrich

  • (A15002)  4-Acetyl-3,5-dimethyl-2-pyrrolecarboxylicacid  95%

  • 2386-28-9

  • A15002-50G

  • 1,477.71CNY

  • Detail

2386-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ACETYL-3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 3-Acetyl-5-carboxy-2,4-dimethyl-pyrrol

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:2386-28-9 SDS

2386-28-9Relevant academic research and scientific papers

Phosphoric acid-promoted synthesis of 4-acylpyrrole-2-carboxylic esters and dipyrryl ketones from mixed anhydrides

Beshara, Cory S.,Thompson, Alison

, p. 10607 - 10610 (2007/10/03)

An efficient synthesis of 4-acylpyrrole-2-carboxylic esters utilizing a phosphoric acid-catalyzed mixed anhydride system is described. The new route also enables the preparation of dipyrryl ketones and N-confused dipyrryl ketones.

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