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1,1'-(1,2-ETHANEDIYL)-BIS-2,5-DIETHYLPYRROLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123147-22-8

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123147-22-8 Usage

Chemical class

Pyrrole derivatives

Formation

Condensation of two molecules of 2,5-diethylpyrrole with 1,2-ethanediamine

Molecular weight

298.47 g/mol

Physical state

Dark-colored, oily liquid

Odor

Characteristic odor

Applications

Organic synthesis, materials science, pharmaceuticals, and agrochemicals development

Check Digit Verification of cas no

The CAS Registry Mumber 123147-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123147-22:
(8*1)+(7*2)+(6*3)+(5*1)+(4*4)+(3*7)+(2*2)+(1*2)=88
88 % 10 = 8
So 123147-22-8 is a valid CAS Registry Number.

123147-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(2,5-diethylpyrrol-1-yl)ethyl]-2,5-diethylpyrrole

1.2 Other means of identification

Product number -
Other names 1,1'-(1,2-Ethanediyl)-bis-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:123147-22-8 SDS

123147-22-8Downstream Products

123147-22-8Relevant academic research and scientific papers

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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