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16200-52-5

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16200-52-5 Usage

Uses

3,4-DIETHYLPYRROLE is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 16200-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16200-52:
(7*1)+(6*6)+(5*2)+(4*0)+(3*0)+(2*5)+(1*2)=65
65 % 10 = 5
So 16200-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N/c1-3-7-5-9-6-8(7)4-2/h5-6,9H,3-4H2,1-2H3

16200-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-diethyl-1H-pyrrole

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole,3,4-diethyl

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:16200-52-5 SDS

16200-52-5Relevant articles and documents

A General Synthesis of Pyrroles from Aldehydes and Ketones

Baldwin, Jack E.,Bottaro, Jeffrey C.

, p. 624 - 625 (1982)

The azines of enolisable aldehydes and ketones are converted into pyrroles via thermal rearrangement of the derived benzoyl derivatives and subsequent hydrazinolysis of the resulting N-benzoylpyrroles.

Regioselective substituent effects upon the synthesis of dipyrrins from 2-formyl pyrroles

Beh, Michael H.R.,Figliola, Carlotta,Lund, Kate-Lyn A.R.,Kajetanowicz, Aleksandra K.,Johnsen, Ann E.,Aronitz, Elise M.,Thompson, Alison

supporting information, p. 779 - 784 (2018/07/06)

The synthesis of symmetric α-free meso-H-dipyrrin hydrobromides from 5-H-2-formyl pyrroles was investigated. The self-condensation produces regioisomeric dipyrrins through adoption of two mechanistic pathways. The key difference between the two pathways lies in which position of the pyrrole directs nucleophilic attack. Through a systematic study involving various substituted and (or) isotopically labelled 5-H-2-formyl pyrroles, we herein provide evidence to suggest that not only do two mechanistic pathways exist, but the steric bulk of the substituent adjacent to the 5-unsubstituted position influences which pathway dominates.

Compound and method of producing organic semiconductor device

-

, (2011/04/26)

A method of producing an organic semiconductor device is provided in which a layer composed of an organic semiconductor having excellent crystallinity and orientation in a low-temperature region can be formed, and the device can be produced in the air. The method includes forming a layer composed of an organic semiconductor precursor on a base body and irradiating the organic semiconductor precursor with light, wherein the organic semiconductor precursor is a porphyrin compound or an azaporphyrin compound having in its molecule at least one of the structure represented by the following general formula (1) or (2):

NOVEL COMPOUND AND METHOD OF PRODUCING ORGANIC SEMICONDUCTOR DEVICE

-

, (2008/12/06)

A method of producing an organic semiconductor device is provided in which a layer composed of an organic semiconductor having excellent crystallinity and orientation in a low-temperature region can be formed, and the device can be produced in the air. The method includes forming a layer composed of an organic semiconductor precursor on a base body and irradiating the organic semiconductor precursor with light, wherein the organic semiconductor precursor is a porphyrin compound or an azaporphyrin compound having in its molecule at least one of the structure represented by the following general formula (1) or (2):

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