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1-(3-Dimethylaminopropyl)-1H-pyrrole-2,5-dione is a chemical compound with the molecular formula C9H14N2O2. It is a derivative of pyrrole, a heterocyclic organic compound consisting of a five-membered aromatic ring with one nitrogen atom and four carbon atoms. In this specific compound, a 3-dimethylaminopropyl group is attached to the nitrogen atom at position 1, and the 2,5-dione functional group is present, indicating the presence of two carbonyl groups at positions 2 and 5. 1-(3-Dimethylaminopropyl)-1H-pyrrole-2,5-dione is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Its chemical structure and properties make it an interesting target for researchers in the field of organic chemistry.

5135-54-6

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5135-54-6 Usage

Chemical structure

A pyrrole-2,5-dione derivative with a dimethylamino group attached to the third carbon of the pyrrole ring and a propyl chain.

Derivation

Derived from pyrrole-2,5-dione, a heterocyclic compound with a nitrogen atom in the ring.

Functional groups

Contains a dimethylamino group (-N(CH3)2) and a propyl chain (-CH2CH2CH3).

Reactivity

Acts as a nucleophile due to the presence of the dimethylamino group, which is an electron-donating group.

Complex formation

Forms stable complexes with various metal ions, making it useful in coordination chemistry.

Applications

Commonly used as a reagent in organic synthesis, particularly for the creation of pharmaceutical compounds and agrochemicals.

Building block

Serves as a building block for the synthesis of various heterocycles and complex organic molecules.

Biological activity

Studied for its potential biological activity, particularly in the field of medicinal chemistry.

Solubility

Soluble in polar solvents such as water, methanol, and ethanol due to the presence of the polar dimethylamino group.

Stability

Relatively stable under normal conditions, but sensitive to strong acids and bases, which can lead to hydrolysis or other degradation reactions.

Hazards

May be harmful if inhaled, ingested, or absorbed through the skin. It is important to handle 1-(3-Dimethylaminopropyl)-1H-pyrrole-2,5-dione with proper safety precautions, such as wearing gloves and using a fume hood.

Storage

Should be stored in a cool, dry place, away from light and heat, and in a sealed container to prevent degradation or contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 5135-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5135-54:
(6*5)+(5*1)+(4*3)+(3*5)+(2*5)+(1*4)=76
76 % 10 = 6
So 5135-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O2/c1-10(2)6-3-7-11-8(12)4-5-9(11)13/h4-5H,3,6-7H2,1-2H3

5135-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(dimethylamino)propyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names DM-Pam

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:5135-54-6 SDS

5135-54-6Upstream product

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