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2H-Imidazol-2-one, 1,3-dihydro-4-(2-nitrobenzoyl)- is a chemical compound with the molecular formula C10H8N2O4. It is a derivative of imidazolone, featuring a 2-nitrobenzoyl group attached to the 4-position of the imidazole ring. 2H-Imidazol-2-one,1,3-dihydro-4-(2-nitrobenzoyl)- is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting various biological processes. Its structure, which includes a nitro group on the benzene ring, may contribute to its reactivity and interaction with biological targets. The compound's properties, such as solubility and stability, can be influenced by the presence of the nitro group, making it a subject of interest for further chemical and biological studies.

849454-35-9

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849454-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849454-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,4,5 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849454-35:
(8*8)+(7*4)+(6*9)+(5*4)+(4*5)+(3*4)+(2*3)+(1*5)=209
209 % 10 = 9
So 849454-35-9 is a valid CAS Registry Number.

849454-35-9SDS

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 4-(2-Nitrobenzoyl)-1,3-dihydro-2H-imidazol-2-one

1.2 Other means of identification

Product number -
Other names -

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:849454-35-9 SDS

849454-35-9Relevant academic research and scientific papers

Hydantoins, triazolones, and imidazolones as selective non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)

Sheppeck II, James E.,Gilmore, John L.,Tebben, Andrew,Xue, Chu-Biao,Liu, Rui-Qin,Decicco, Carl P.,Duan, James J.-W.

, p. 2769 - 2774 (2008/02/05)

We have discovered selective and potent inhibitors of TACE that replace the common hydroxamate zinc binding group with a hydantoin, triazolone, and imidazolone heterocycle. These novel heterocyclic inhibitors of a zinc metalloprotease were designed using

Substituted 1,3-dihydro-imidazol-2-one and 1,3-dihydro-imidazol-2-thione derivatives as inhibitors of matrix metalloproteinases and/or TNF-alpha converting enzyme (TACE)

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Page/Page column 17, (2010/02/11)

The present invention describes novel 1,3-dihydro-imidazol-2-one or 1,3-dihydro-imidazol-2-thione compounds of formula (I): or a stereoisomer or pharmaceutically acceptable salt or solvate thereof, wherein A, L R1, R2, R3

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