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Ethyl 4-iodo-3,5-dimethyl-1H-pyrrole-2-carboxylate is a chemical compound with the molecular formula C9H12INO2. It is a derivative of pyrrole, a heterocyclic organic compound with a five-membered ring containing four carbon atoms and one nitrogen atom. In this specific compound, the pyrrole ring is substituted with an ethyl group at the 2-position (the carbonyl group), a methyl group at the 3-position, another methyl group at the 5-position, and an iodine atom at the 4-position. ethyl 4-iodo-3,5-dimethyl-1H-pyrrole-2-carboxylate is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions, such as the reaction of 4-iodo-3,5-dimethyl-1H-pyrrole-2-carboxylic acid with ethanol in the presence of a coupling agent. The compound is soluble in organic solvents and has potential applications in the development of new drugs and other chemical products.

5408-08-2

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5408-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5408-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5408-08:
(6*5)+(5*4)+(4*0)+(3*8)+(2*0)+(1*8)=82
82 % 10 = 2
So 5408-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12INO2/c1-4-13-9(12)8-5(2)7(10)6(3)11-8/h11H,4H2,1-3H3

5408-08-2SDS

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 ethyl 4-iodo-3,5-dimethyl-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 4-iodo-3,5-dimethyl-pyrrole-2-carboxylic acid ethyl ester

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

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More Details:5408-08-2 SDS

5408-08-2Relevant academic research and scientific papers

Molecular Features of the YAP Inhibitor Verteporfin: Synthesis of Hexasubstituted Dipyrrins as Potential Inhibitors of YAP/TAZ, the Downstream Effectors of the Hippo Pathway

Gibault, Floriane,Bailly, Fabrice,Corvaisier, Matthieu,Coevoet, Mathilde,Huet, Guillemette,Melnyk, Patricia,Cotelle, Philippe

, p. 954 - 961 (2017/06/27)

Porphyrin derivatives, in particular verteporfin (VP), a photosensitizer initially designed for cancer therapy, have been identified as inhibitors of the YAP–TEAD interaction and transcriptional activity. Herein we report the efficient convergent synthesis of the dipyrrin half of protoporphyrin IX dimethyl ester (PPIX-DME), in which the sensitive vinyl group was created at the final stage by a dehydroiodination reaction. Two other dipyrrin derivatives were synthesized, including dipyrrin 19 [(Z)-2-((3,5-dimethyl-4-vinyl-2H-pyrrol-2-ylidene)methyl)-3,5-dimethyl-4-vinyl-1H-pyrrole], containing two vinyl groups. We found that VP and dipyrrin 19 showed significant inhibitory effects on TEAD transcriptional activity in MDA-MB-231 human breast cancer cells, whereas other compounds did not show significant changes. In addition, we observed a marked decrease in both YAP and TAZ levels following VP treatment, whereas dipyrrin 19 treatment primarily decreased the levels of YAP and receptor kinase AXL, a downstream target of YAP. Together, our data suggest that, due to their chemical structures, porphyrin- and dipyrrin-related derivatives can directly target YAP and/or TAZ proteins and inhibit TEAD transcriptional activity.

THALLIUM AND MERCURY IN PYRROLE CHEMISTRY. USE OF C-THALLIATED AND C-MERCURIATED PYRROLE DERIVATIVES FOR SELECTIVE RING FUNCTIONALISATIONS via ipso-DETHALLIATION AND -DEMERCURIATION REACTIONS

Monti, Donato,Sleiter, Giancarlo

, p. 771 - 774 (2007/10/02)

The use of C-thalliated and C-mercuriated pyrroles to achieve selective introduction of various functional groups in a β position is described.High yields of hardly accessible pyrrole derivatives (such as nitropyrrole) can thus be obtained.

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