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2-Nitro-1-(p-nitrobenzyl)-1H-imidazole is a chemical compound with the molecular formula C9H7N3O4. It is a versatile molecule known for its strong binding affinity to nucleic acids, making it a valuable tool in molecular biology and biochemistry research.

10598-82-0

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10598-82-0 Usage

Uses

Used in Molecular Biology and Biochemistry Research:
2-Nitro-1-(p-nitrobenzyl)-1H-imidazole is used as a histological dye for visualizing proteins and nucleic acids in biological samples. Its strong binding affinity to nucleic acids makes it a useful tool in these research fields.
Used in Antitumor and Anticancer Research:
2-Nitro-1-(p-nitrobenzyl)-1H-imidazole is being investigated for its potential antitumor and anticancer properties. Its effectiveness in these areas is still under study, and further research is needed to fully understand its capabilities as a therapeutic agent.
Used in Photodynamic Therapy:
2-Nitro-1-(p-nitrobenzyl)-1H-imidazole has also been explored for its use as a photosensitizer in photodynamic therapy. This application is still in the research phase, and more work is required to determine its full potential in this medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 10598-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,9 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10598-82:
(7*1)+(6*0)+(5*5)+(4*9)+(3*8)+(2*8)+(1*2)=110
110 % 10 = 0
So 10598-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N4O4/c15-13(16)9-3-1-8(2-4-9)7-12-6-5-11-10(12)14(17)18/h1-6H,7H2

10598-82-0SDS

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-nitro-1-[(4-nitrophenyl)methyl]imidazole

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:10598-82-0 SDS

10598-82-0Downstream Products

10598-82-0Relevant academic research and scientific papers

SRN1 AND OXIDATIVE ADDITION REACTIONS OF NITROIMIDAZOLE ANIONS

Adebayo, Adelaide T. O. M.,Bowman, Russell,Salt, W. G.

, p. 1943 - 1946 (2007/10/02)

The anions of 2- and 4(5)-nitroimidazoles react with aliphatic substituted nitro compounds and p-nitrobenzyl chloride by a SRN1 mechanism, or by oxidative addition to the anion of 2-nitropropane, to yield 1-alkyl-2-(or 4-)-nitroimidazoles.

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