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21407-88-5

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21407-88-5 Usage

Chemical class

Aromatic heterocyclic organic compound, consisting of a five-membered ring with four carbon atoms and one nitrogen atom.

Structural features

Two ethyl groups and one isopropyl group attached to the pyrrole ring.

Usage in organic synthesis

Serves as a building block for the synthesis of various biologically active compounds.

Pharmaceutical research

Potential applications in the development of new drugs due to its pharmacological properties.

Pharmacological properties

Exhibits antifungal and antimicrobial effects, making it a compound of interest for potential therapeutic uses.

Field of applications

Chemistry and pharmacology, owing to its unique structural characteristics and potential biological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 21407-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,0 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21407-88:
(7*2)+(6*1)+(5*4)+(4*0)+(3*7)+(2*8)+(1*8)=85
85 % 10 = 5
So 21407-88-5 is a valid CAS Registry Number.

21407-88-5SDS

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 2,5-diethyl-1-propan-2-ylpyrrole

1.2 Other means of identification

Product number -
Other names 1-isopropyl-2,5-diethylpyrrole

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:21407-88-5 SDS

21407-88-5Downstream Products

21407-88-5Relevant articles and documents

An Electron Spin Resonance Study of the Radical Cations of Pyrroles, Furans, and Thiophenes in Liquid Solution

Davies, Alwyn G.,Julia, Luis,Yazdi, Safieh N.

, p. 239 - 244 (2007/10/02)

Photolysis of alkylpyrroles in trifluoroacetic acid containing mercury(II) trifluoroacetate, alkylfurans in trifluoroacetic acid, or alkylthiophenes in sulphuric acid, induces oxidation to the corresponding radical cations.The e.s.r. spectra show that the electronic configuration is similar in all three species, the unpaired electron occupying the φA MO in which the heteroatom lies in a nodal plane.Photolysis of 2,6-dimethyl- and 2,6-diethyl-thiophene in trifluoroacetic acid containing mercury(II) trifluoroacetate, on the other hand, gave rise to spectra with a high g value (2.0062), showing hyperfine coupling to two non-equivalent pairs of alkyl groups in an unsymmetrical dimer.

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