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53013-38-0

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53013-38-0 Usage

Description

2-Nitrophenyl Diphenylamine (CAS# 53013-38-0) is an organic compound characterized by its orange powder appearance. It is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the creation of various chemical products.

Uses

Used in Organic Synthesis:
2-Nitrophenyl Diphenylamine is used as a synthetic intermediate for the production of a range of chemical compounds. Its unique structure and properties make it a versatile building block in the synthesis of various organic molecules, contributing to the development of new materials and substances with potential applications in different industries.
Used in Chemical Research:
In the field of chemical research, 2-Nitrophenyl Diphenylamine serves as a valuable compound for studying the properties and behavior of organic molecules. Its distinctive characteristics allow researchers to gain insights into the mechanisms of various chemical reactions and processes, ultimately leading to a deeper understanding of organic chemistry and the development of innovative solutions in the field.
Used in Pharmaceutical Industry:
2-Nitrophenyl Diphenylamine is also employed in the pharmaceutical industry as a key component in the synthesis of certain drugs and pharmaceutical compounds. Its unique properties and reactivity enable the creation of new therapeutic agents with potential applications in the treatment of various diseases and medical conditions.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 2-Nitrophenyl Diphenylamine is utilized for the production of specific dyes and pigments. Its orange powder form contributes to the development of vibrant and stable colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Analytical Chemistry:
2-Nitrophenyl Diphenylamine is also used in analytical chemistry as a reagent or indicator in certain analytical techniques. Its distinct properties allow for the accurate detection and quantification of specific substances, enhancing the efficiency and reliability of analytical processes in research and quality control settings.

Check Digit Verification of cas no

The CAS Registry Mumber 53013-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,1 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53013-38:
(7*5)+(6*3)+(5*0)+(4*1)+(3*3)+(2*3)+(1*8)=80
80 % 10 = 0
So 53013-38-0 is a valid CAS Registry Number.

53013-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Nitro-N,N-diphenylaniline

1.2 Other means of identification

Product number -
Other names N.N-Diphenyl-2-nitro-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:53013-38-0 SDS

53013-38-0Relevant articles and documents

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Gomberg,Kamm

, p. 2009 (1917)

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Substituent effects on the redox properties and structure of substituted triphenylamines. An experimental and computational study

Wu, Xin,Davis, Anthony P.,Lambert, Peter C.,Kraig Steffen,Toy, Ozan,Fry, Albert J.

experimental part, p. 2408 - 2414 (2009/07/18)

The peak oxidation potentials of a series of polysubstituted triphenylamines were found to be highly linearly correlated (R=0.995) with their ionization potentials as computed by density functional theory. The computations, as well as confirming previous

Nitration of the Acetanilide-type Compounds

Daszkiewicz, Zdzislaw,Kyziol, Janusz B.

, p. 44 - 50 (2007/10/02)

Some aromatic compounds containing the imino group (NH) were nitrated in acetic acid or anhydride, and the ortho/para ratios were measured.N-Methyl derivatives of the aforementioned compounds are much less reactive when nitrated under comparable conditions and give significantly lower o/p ratios.These results along with the literature data support the hypothesis that the acetanilide-type compounds are nitrated via N-nitro intermediates.

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