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5-Pyrimidinecarboxamide, N-methoxy-N-methylis a chemical compound with the molecular formula C7H8N4O2. It is a derivative of pyrimidinecarboxamide, containing both a methoxy and a methyl group. 5-Pyrimidinecarboxamide, N-methoxy-N-methylhas significant potential applications in drug discovery and development due to its unique structure and properties.

823189-68-0

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823189-68-0 Usage

Uses

Used in Pharmaceutical Industry:
5-Pyrimidinecarboxamide, N-methoxy-N-methylis used as a building block for the synthesis of various drugs and pharmaceuticals. Its presence as an intermediate in the preparation of numerous bioactive molecules makes it an important component in drug development.
Used in Scientific Research:
5-Pyrimidinecarboxamide, N-methoxy-N-methylis also used as a research chemical in scientific studies and experiments. Its unique structure allows researchers to explore its properties and potential applications in various fields of chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 823189-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,1,8 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 823189-68:
(8*8)+(7*2)+(6*3)+(5*1)+(4*8)+(3*9)+(2*6)+(1*8)=180
180 % 10 = 0
So 823189-68-0 is a valid CAS Registry Number.

823189-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methoxy-N-methylpyrimidine-5-carboxamide

1.2 Other means of identification

Product number -
Other names 5-PyriMidinecarboxaMide,N-Methoxy-N-Methyl

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:823189-68-0 SDS

823189-68-0Relevant academic research and scientific papers

METALLOENZYME INHIBITOR COMPOUNDS AS FUNGICIDES

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Paragraph 00245, (2015/11/09)

The instant invention describes compounds of Formula I having metalloenzyme modulating activity, and methods of treating diseases disorders or symptoms thereof mediated by such metalloenzymes.

One-Pot Direct Synthesis of Weinreb Amides from Aryl and Hetero Aryl Halides Using Co 2(CO) 8 as an Effective CO Source under Conventional Thermal Heating

Baburajan, Poongavanam,Elango, Kuppanagounder P.

, p. 541 - 548 (2015/10/29)

A successful protocol for the synthesis of Weinreb amides directly from aryl halides via aminocarbonylation with N,O-dimethyl hydroxylamine using Co2(CO)8 as an in situ CO source has been demonstrated. The effects of various reaction parameters such as temperature, base, and CO source have also been investigated and optimized. GRAPHICAL ABSTRACT.

HETEROARYL LINKED QUINOLINYL MODULATORS OF RORyt

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Paragraph 0342; 0343, (2014/05/07)

The present invention comprises compounds of Formula I. wherein: R1, R2, R3, R4, R5, R6, R7, R8, and R9 are defined in the specification. The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of claim 1.

An Efficient synthesis of Weinreb amides and ketones via palladium nanoparticles on ZIF-8 catalysed carbonylative coupling

Thanh Dang, Tuan,Chen, Anqi,Majeed Seayad, Abdul

, p. 30019 - 30027 (2014/08/05)

Heterogeneously catalysed carbonylative coupling reactions such as aminocarbonylation and Suzuki-carbonylation are reported using Pd nanoparticles supported on ZIF-8 for efficient and environmentally attractive synthesis of Weinreb amides and ketones from aryl bromides or iodides. The catalyst is air stable, offers high activity with very low palladium leaching and is recyclable. The presence of a phosphine ligand was required when aryl bromides were used as substrates, while no ligand was necessary when aryl iodides were used. the Partner Organisations 2014.

TACHYKININ RECEPTOR ANTAGONISTS

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Page 54, (2010/02/10)

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.

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