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2,4-Dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid ethyl ester is a chemical compound with the molecular formula C12H17NO3. It is an ethyl ester derivative of 2,4-dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid, known for its unique structure and properties. 2,4-Dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid ethyl ester is commonly used in biochemical research as a probe for the identification and characterization of target proteins. Additionally, it has potential pharmaceutical and therapeutic applications, particularly in the development of anti-inflammatory and anti-cancer drugs.

78956-69-1

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78956-69-1 Usage

Uses

Used in Biochemical Research:
2,4-Dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid ethyl ester is used as a probe for the identification and characterization of target proteins. Its unique structure allows for specific interactions with proteins, making it a valuable tool in understanding protein functions and mechanisms.
Used in Pharmaceutical Development:
2,4-Dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid ethyl ester is used as a potential candidate in the development of anti-inflammatory and anti-cancer drugs. Its properties and interactions with biological systems make it a promising compound for the creation of new therapeutic agents.
Used in Medical Research:
2,4-Dimethyl-5-(1-oxopropyl)1H-pyrrole-3-carboxylic acid ethyl ester is used in medical research to explore its potential applications in various scientific and medical fields. Its unique properties and interactions with biological systems contribute to the advancement of knowledge in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 78956-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,5 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78956-69:
(7*7)+(6*8)+(5*9)+(4*5)+(3*6)+(2*6)+(1*9)=201
201 % 10 = 1
So 78956-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO3/c1-5-9(14)11-7(3)10(8(4)13-11)12(15)16-6-2/h13H,5-6H2,1-4H3

78956-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-Formylmethyl)-2,3-dimethyl-3-pyrrolcarbonsaeure-ethylester

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-5-(3-oxo-propyl)-1H-pyrrole-3-carboxylic acid ethyl ester

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:78956-69-1 SDS

78956-69-1Downstream Products

78956-69-1Relevant academic research and scientific papers

Reactions of Pyrroles with α,β-Unsaturated Aldehydes and Ketones

Treibs, Alfred,Wilhelm, Roland,Hermann, Erwin

, p. 849 - 857 (2007/10/02)

Reactions of α,β-unsaturated aldehydes and ketones with pyrrole derivatives yields the (3-oxoalkyl)pyrroles 2, 6 and 7 as well as the tris(pyrrolyl)propanes 3 and 4.Compound 3a is oxidized to give the tripyrryltrimethine 5 and the dipyrryltrimethine 1a, respectively.The Bucherer hydantoin reaction is recognized to be suitable for the characterization of (3-oxoalkyl)pyrroles.

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