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4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is a chemical compound characterized by a pyrrole ring and a carboxylic acid group. It is defined by its molecular formula C11H13NO3 and possesses a molar mass of 207.23 g/mol. 4-ACETYL-3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID is notable for its potential applications in medicinal chemistry and the production of dyes and pigments, owing to its reactive nature and versatile chemistry.

2386-33-6

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2386-33-6 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical properties and structural features make it a valuable component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Compounds Synthesis:
4-ACETYL-3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID also serves as a building block in the synthesis of a range of organic compounds, leveraging its reactivity and structural attributes to create diverse chemical entities for various applications.
Used in Dyes and Pigments Production:
Due to its reactive nature, 4-acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid is employed as a starting material in the production of dyes and pigments. Its versatile chemistry allows for the creation of a spectrum of colorants used across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2386-33-6 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, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2386-33:
(6*2)+(5*3)+(4*8)+(3*6)+(2*3)+(1*3)=86
86 % 10 = 6
So 2386-33-6 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)

2386-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-acetyl-4,5-dimethyl-2-pyrrole 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:2386-33-6 SDS

2386-33-6Downstream Products

2386-33-6Relevant academic research and scientific papers

PREPARATION OF 4,5-DIALKYL-3-ACYL-PYRROLE-2-CARBOXYLIC ACID DERIVATIVES BY FISCHER-FINK TYPE SYNTHESIS AND SUBSEQUENT ACYLATION

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Page/Page column 24-26, (2008/06/13)

The present invention relates to an improved synthesis of pyrrole capping group precursors of formula I-a: comprising: combining an aqueous solution of the compound of formula IV-a: wherein R3 is C1-12 aliphatic, C3-12 alkyl-cycloaliphatic, C3-12 alkyl-aryl, C3-12 alkyl-heteroaryl, or C3-12 alkyl-cycloaliphatic; with a compound of formula V-a, wherein R1 and R2 are each independently C1-6 aliphatic; in the presence of zinc, water, and optionally an additional suitable solvent to form a compound of formula VI.

Inhibitors of serine proteases, particularly HCV NS3-NS4A protease

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, (2008/06/13)

The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antivi

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