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5-Nitro-1,3-benzodioxol-2-one is a chemical compound with the molecular formula C7H5NO5. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 5-nitro-1,3-benzodioxol-2-one is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing the benzodioxole moiety. It is also used in the preparation of dyes and pigments. Due to its reactivity, it is essential to handle 5-nitro-1,3-benzodioxol-2-one with care, as it may pose health risks and environmental concerns.

25859-54-5

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25859-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25859-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25859-54:
(7*2)+(6*5)+(5*8)+(4*5)+(3*9)+(2*5)+(1*4)=145
145 % 10 = 5
So 25859-54-5 is a valid CAS Registry Number.

25859-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-1,3-benzodioxol-2-one

1.2 Other means of identification

Product number -
Other names 1,3-Benzodioxol-2-one,5-nitro

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:25859-54-5 SDS

25859-54-5Relevant academic research and scientific papers

Catechol-appended TTF derivatives

El-Ghayoury, Abdelkrim,Leliège, Antoine,Allain, Magali,Batail, Patrick

, p. 4015 - 4018 (2013/07/26)

EDT-TTF-CONHCatOH, a catechol-appended TTF derivative, 5 was synthesized through a straightforward strategy. The electronic absorption and the electrochemical investigations as well as molecular orbital calculations for compounds 4 and 5 have been performed. The electrochemical measurements of 5 indicate that it is a suitable candidate for the formation of zwitterionic molecular solids and also two-component radical cation salts. The crystal structure of compound 5 reveals supramolecular dimers assembled via a set of O-H?O hydrogen bonds between the catechol and amide units.

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