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5-Methoxy-2,4-dinitroaniline is an organic compound with the chemical formula C7H7N3O5. It is a yellow crystalline solid that is soluble in water and various organic solvents. 5-methoxy-2,4-dinitroaniline is characterized by the presence of a methoxy group (-OCH3) at the 5th position, and two nitro groups (-NO2) at the 2nd and 4th positions of the aniline (C6H5NH2) backbone. 5-Methoxy-2,4-dinitroaniline is primarily used as a chemical intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Due to its reactivity and potential applications, it is essential to handle 5-methoxy-2,4-dinitroaniline with care, as it may pose health and environmental risks.

7072-80-2

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7072-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7072-80-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7072-80:
(6*7)+(5*0)+(4*7)+(3*2)+(2*8)+(1*0)=92
92 % 10 = 2
So 7072-80-2 is a valid CAS Registry Number.

7072-80-2SDS

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 5-methoxy-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names 2,4-dinitro-5-methoxyaniline

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:7072-80-2 SDS

7072-80-2Relevant academic research and scientific papers

A reverse method for diversity introduction of benzimidazole to synthesize H+/K+-ATP enzyme inhibitors

Yan, Yu,Liu, Zijie,Zhang, Jianjun,Xu, Ruiming,Hu, Xiao,Liu, Gang

supporting information; experimental part, p. 4189 - 4192 (2011/08/10)

A series of 2-[(2-pyridylmethyl)sulfinyl]benzimidazole derivatives were synthesized via a solution phase synthetic route using a reversal method of diversity introduction. Using this synthetic strategy, we obtained two key intermediates (4-A and 4-B) simultaneously, which allows us to introduce diversity points onto the benzimidazole part of the final product under reliable reaction conditions to identify potent H+/K+-ATP enzyme inhibitors. Compound 14l (IC50 = 1.6 × 10-5 M) was comparable with H+/K+-ATP enzyme inhibitor in vitro.

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