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368211-06-7

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368211-06-7 Usage

Derivative of pyrrole

A five-membered aromatic heterocycle The compound is based on a pyrrole structure, which is a five-membered ring containing one nitrogen atom and four carbon atoms.

Carboxamide functional group

A nitrogen atom with an attached amide group The compound contains an amide group (C=O) bonded to a nitrogen atom, which is a common functional group in organic synthesis and medicinal chemistry.

Methoxy and methyl substituents

Two organic groups attached to the nitrogen atom A methoxy group (-OCH3) and a methyl group (-CH3) are present on the nitrogen atom, which can influence the compound's reactivity and properties.

Building block in organic synthesis

Versatile starting material for creating more complex molecules The compound can be used as a starting material to synthesize a variety of more complex organic molecules, making it valuable in research and industrial applications.

Medicinal chemistry applications

Potential use in the development of pharmaceuticals Due to its unique structure and functional groups, 1H-Pyrrole-2-carboxamide, N-methoxy-N-methyl (9CI) may be used in the design and synthesis of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 368211-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,8,2,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 368211-06:
(8*3)+(7*6)+(6*8)+(5*2)+(4*1)+(3*1)+(2*0)+(1*6)=137
137 % 10 = 7
So 368211-06-7 is a valid CAS Registry Number.

368211-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-pyrrole-2-carboxylic acid methoxymethylamide

1.2 Other means of identification

Product number -
Other names N-methoxy-N-methyl-1H-pyrrole-2-carboxamide

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:368211-06-7 SDS

368211-06-7Relevant articles and documents

MCL-1 MODULATING COMPOSITIONS

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Page/Page column 33; 34; 35; 52; 53, (2013/08/15)

The present invention relates to marinopyrrole A derivatives and pyoluteorin derivatives and methods of treatment of disorders associated with misregulation of Mcl-l, e.g., leukemia, lymphoma, multiple myeloma, melanoma, or pancreatic cancer. We describe exemplary compounds, which may be contained in pharmaceutical compositions, and their use as therapeutic agents either alone or in combination with other anti-cancer treatments, e.g., anti-Bcl- 2 agents.

Total synthesis of (±)-marinopyrrole a via copper-mediated N-arylation

Kanakis, Argyrios A.,Sarli, Vasiliki

supporting information; experimental part, p. 4872 - 4875 (2011/02/22)

The total synthesis of the racemic form of the marine alkaloid marinopyrrole A is described. The characteristic 1,3′-bipyrrole core was constructed by a copper-mediated N-arylation process under microwave irradiation.

Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis

-

, (2008/06/13)

Compounds of the formula: where the formula variables are as defined in the disclosure, advantageously inhibit or block the biological activity of the picomaviral 3C protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with one or more picomaviruses, such as RVP. Intermediates and synthetic methods for preparing such compounds are also described.

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