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887694-84-0

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887694-84-0 Usage

General Description

2,5-dimethyl-1-(2-morpholin-4-ylethyl)-1H-pyrrole-3-carbaldehyde is a chemical compound with the molecular formula C13H17NO2. It is a pyrrole derivative with a morpholine ring attached to the second carbon atom and a aldehyde group attached to the third carbon atom. 2,5-dimethyl-1-(2-morpholin-4-ylethyl)-1H-pyrrole-3-carbaldehyde is commonly used in organic synthesis and pharmaceutical research due to its potential medicinal properties. It has been studied for its potential as an anti-cancer and anti-inflammatory agent, as well as its ability to act as an inhibitor for certain enzymes. Additionally, it has been used as a building block for the synthesis of various pharmacologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 887694-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,6,9 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 887694-84:
(8*8)+(7*8)+(6*7)+(5*6)+(4*9)+(3*4)+(2*8)+(1*4)=260
260 % 10 = 0
So 887694-84-0 is a valid CAS Registry Number.

887694-84-0SDS

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 2,5-Dimethyl-1-(2-morpholin-4-yl-ethyl)-1H-pyrrole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,5-dimethyl-1-(2-morpholinoethyl)-1H-pyrrole-3-carbaldehyde

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:887694-84-0 SDS

887694-84-0Downstream Products

887694-84-0Relevant articles and documents

Discovery and optimisation studies of antimalarial phenotypic hits

Mital, Alka,Murugesan, Dinakaran,Kaiser, Marcel,Yeates, Clive,Gilbert, Ian H.

, p. 530 - 538 (2015/10/12)

There is an urgent need for the development of new antimalarial compounds. As a result of a phenotypic screen, several compounds with potent activity against the parasite Plasmodium falciparum were identified. Characterization of these compounds is discussed, along with approaches to optimise the physicochemical properties. The in vitro antimalarial activity of these compounds against P. falciparum K1 had EC50 values in the range of 0.09e29 mM, and generally good selectivity (typically >100-fold) compared to a mammalian cell line (L6). One example showed no significant activity against a rodent model of malaria, and more work is needed to optimise these compounds.

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