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1H-Pyrrole-2-carboxamide, N-ethyl (9CI) is a chemical compound characterized by the molecular formula C8H10N2O. It is a derivative of the heterocyclic organic compound pyrrole, featuring an amide group and an ethyl substituent. 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI) is of interest in pharmaceutical research due to its potential biological activity and is currently under investigation for its possible medicinal properties.

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  • 156741-80-9 Structure
  • Basic information

    1. Product Name: 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI)
    2. Synonyms: 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI);N-Ethyl-1H-pyrrole-2-carboxamide
    3. CAS NO:156741-80-9
    4. Molecular Formula: C7H10N2O
    5. Molecular Weight: 138.1671
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 156741-80-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Room temperature.
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI)(156741-80-9)
    11. EPA Substance Registry System: 1H-Pyrrole-2-carboxamide,N-ethyl-(9CI)(156741-80-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 156741-80-9(Hazardous Substances Data)

156741-80-9 Usage

Uses

Used in Pharmaceutical Research:
1H-Pyrrole-2-carboxamide, N-ethyl (9CI) is utilized as a research compound for exploring its potential biological activity. It is being studied for its possible applications in the development of new drugs or treatments for various medical conditions.
Used in Drug Development:
In the pharmaceutical industry, 1H-Pyrrole-2-carboxamide, N-ethyl (9CI) is used as a lead compound in the discovery and design of novel therapeutic agents. Its unique structure and properties may contribute to the creation of medications that address unmet medical needs.
Further research and testing are essential to fully understand the potential uses and effects of 1H-Pyrrole-2-carboxamide, N-ethyl (9CI), ensuring its safety and efficacy in any proposed applications.

Check Digit Verification of cas no

The CAS Registry Mumber 156741-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,4 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156741-80:
(8*1)+(7*5)+(6*6)+(5*7)+(4*4)+(3*1)+(2*8)+(1*0)=149
149 % 10 = 9
So 156741-80-9 is a valid CAS Registry Number.

156741-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-1H-pyrrole-2-carboxamide

1.2 Other means of identification

Product number -
Other names N-ethyl-1H-pyrrole-2-carboxamide

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:156741-80-9 SDS

156741-80-9Downstream Products

156741-80-9Relevant articles and documents

Selective synthesis of N-substituted pyrrolo[1,2-a]pyrazin-1(2H)-one derivatives via alkyne cyclization

?etinkaya, Yasin,Balci, Metin

, p. 6698 - 6702 (2014)

A novel and efficient synthesis of N-substituted pyrrolo-pyrazinone derivatives has been developed. A trichloroacetyl group connected to the pyrrole ring was converted into the desired carboxamide derivatives. Promoted by NaH, the pyrrole carboxamide derivatives underwent a tandem reaction with propargyl bromide to afford pyrrolo-pyrazinones with high efficiency under very mild conditions. The mechanism for the formation of the products is discussed and supported by DFT calculations.

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