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216591-43-4

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216591-43-4 Usage

Nitro derivative of pyrrole

The compound is derived from pyrrole, a five-membered aromatic ring with one nitrogen atom, by introducing a nitro group (-NO2) into its structure.

Reactivity

Highly reactive The presence of the nitro group makes the compound more reactive, which can lead to potential hazards when handling or storing it.

Potentially explosive

The compound's reactivity increases its risk of being explosive under certain conditions, so it must be handled and stored with extreme caution.

Uses

Intermediate in the synthesis of various organic compounds 1H-Pyrrole,1-ethyl-3-nitro-(9CI) is primarily used as an intermediate in the production of other organic compounds, such as pharmaceuticals and agrochemicals.

Health hazards

Potential health risks Due to its chemical nature, the compound may pose health hazards if not handled and stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 216591-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,5,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 216591-43:
(8*2)+(7*1)+(6*6)+(5*5)+(4*9)+(3*1)+(2*4)+(1*3)=134
134 % 10 = 4
So 216591-43-4 is a valid CAS Registry Number.

216591-43-4SDS

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 1-ethyl-3-nitropyrrole

1.2 Other means of identification

Product number -
Other names 1-Ethyl-3-nitro-1H-pyrrole

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:216591-43-4 SDS

216591-43-4Downstream Products

216591-43-4Relevant articles and documents

TETRAHYDROQUINOLINE DERIVATIVES AND THE USE THEREOF FOR THE TREATMENT OF CANCER

-

Page/Page column 14, (2010/04/23)

Compounds of the formula (I), in which E, R3, R4, R5, X, Y, W, Q1, Q2, Z, s and m have the meanings indicated in claim 1, can be employed, inter alia, for the treatment of tumours.

Electrochemically induced N-alkylation of pyrroles

Feroci, Marta,Inesi, Achille,Rossi, Leucio,Sleiter, Giancarlo

, p. 955 - 958 (2007/10/03)

Electrochemically generated tetraethylammonium peroxydicarbonate (TEAPC) and tetraethylammonium carbonate (TEAC) react under very mild conditions with pyrroles affording, after addition of a suitable alkylating agent, the corresponding N-alkylated pyrrole

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