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3-Nitronaphthalene-1,2-dione is an organic compound with the chemical formula C10H5NO4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 3-nitronaphthalene-1,2-dione is an important intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. It is synthesized through various methods, including nitration of naphthalene-1,2-dione and oxidation of 3-aminonaphthalene-1,2-dione. Due to its reactivity, 3-nitronaphthalene-1,2-dione is used in the preparation of various derivatives, such as 3-aminonaphthalene-1,2-dione and 3-hydroxynaphthalene-1,2-dione, which have applications in the chemical and pharmaceutical industries.

7474-84-2

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7474-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7474-84-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7474-84:
(6*7)+(5*4)+(4*7)+(3*4)+(2*8)+(1*4)=122
122 % 10 = 2
So 7474-84-2 is a valid CAS Registry Number.

7474-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitronaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 3-Nitronaphthochinon-(1,2)

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:7474-84-2 SDS

7474-84-2Relevant academic research and scientific papers

Research on antitumor chemotherapy: X. β Nitrostyrene and nitrovinyl derivatives

Dore,Viel

, p. 81 - 109 (2007/10/06)

In previous work, the antitumoral cytotoxicity of β nitrostyrenes obtained by simplification of the aristolochic acid molecule was demonstrated. The effect of modifying the 3 characteristic parts of the β nitrostyrene molecule was then investigated. Results in vitro and in vivo indicate a probable mechanism of action for the β nitrostyrene and nitrovinyl compounds studied, and permit definition of the maximum simplification compatible with retention of biological activity.

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