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2,4-dinitro-N-(1-phenylethyl)aniline, also known as Dinilin, is a chemical compound with the molecular formula C14H13N3O4. It is a nitroaniline, which is a type of aromatic amine, and is characterized by its yellowish solid appearance. 2,4-dinitro-N-(1-phenylethyl)aniline is primarily used as a dye intermediate in the production of synthetic dyes.

31493-50-2

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31493-50-2 Usage

Uses

Used in Textile Industry:
2,4-dinitro-N-(1-phenylethyl)aniline is used as a dye intermediate for the manufacturing of azo dyes, which are extensively utilized in the textile industry. These dyes are known for their vibrant colors and are applied to fabrics to create a wide range of hues and patterns.
Used in Chemical Industry:
2,4-dinitro-N-(1-phenylethyl)aniline is used as a chemical intermediate in the synthesis of various other compounds. Its role in the chemical industry is to facilitate the production of a range of products that may have applications in different sectors.
Safety Considerations:

Check Digit Verification of cas no

The CAS Registry Mumber 31493-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,9 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31493-50:
(7*3)+(6*1)+(5*4)+(4*9)+(3*3)+(2*5)+(1*0)=102
102 % 10 = 2
So 31493-50-2 is a valid CAS Registry Number.

31493-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-N-(1-phenyl-ethyl)-aniline

1.2 Other means of identification

Product number -
Other names 2,4-Dinitro-N-(1-phenyl-aethyl)-anilin

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:31493-50-2 SDS

31493-50-2Downstream Products

31493-50-2Relevant academic research and scientific papers

Iron-catalyzed C-C bond cleavage and C-N bond formation

Li, Wenjuan,Zheng, Xiaojian,Li, Zhiping

, p. 181 - 190 (2013/03/13)

A novel approach for C-N bond formation was developed by iron-catalyzed C-C bond cleavage. Anilines and sulfonamides reacted smoothly with 2-substituted 1,3-diphenylpropane-1,3-diones to afford N-alkylation products, in which the 1,3-dicarbonyl group acts as a leaving group in the presence of an iron catalyst. The reversible C-C bond cleavage plays a driving force to give the thermodynamically stable products. The method is complementary to the previous methods for C-N bond formation. Copyright

Direct formation of aromatic C-N bonds. Regioselective amination of m- dinitrobenzene via fluoride promoted nucleophilic aromatic photosubstitution for hydrogen

Huertas, Inma,Gallardo, Iluminada,Marquet, Jordi

, p. 279 - 281 (2007/10/03)

Useful yields are achieved in the regioselective direct formation of anilines and aromatic amides through hydrogen nucleophilic aromatic photosubstitution of m-dinitrobenzene with primary amines and amides, promoted by fluoride anion.

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