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10598-82-0

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10598-82-0 Usage

General Description

2-Nitro-1-(p-nitrobenzyl)-1H-imidazole is a chemical compound with the molecular formula C9H7N3O4. It is commonly used as a histological dye to visualize proteins and nucleic acids in biological samples. 2-Nitro-1-(p-nitrobenzyl)-1H-imidazole is known for its strong binding affinity to nucleic acids, making it a useful tool in molecular biology and biochemistry research. Additionally, 2-Nitro-1-(p-nitrobenzyl)-1H-imidazole has been investigated for its potential antitumor and anticancer properties, as well as its use as a photosensitizer in photodynamic therapy. However, further research is needed to fully understand the biological and medical applications of this chemical.

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10598-82-0 SDS

10598-82-0Downstream Products

10598-82-0Relevant articles and documents

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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