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4-aMino-5-nitrophthalodinitrile is an organic compound that serves as a key intermediate in the synthesis of various pharmaceutical and biologically active compounds. It is characterized by its unique molecular structure, which features an amino group, a nitro group, and a phthalodinitrile moiety. This versatile chemical building block plays a crucial role in the development of novel therapeutic agents and pigments.

79319-38-3

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79319-38-3 Usage

Uses

Used in Pharmaceutical Synthesis:
4-aMino-5-nitrophthalodinitrile is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties allow it to be incorporated into a wide range of drug molecules, enhancing their therapeutic potential and efficacy.
Used in Biologically Active Compounds:
4-aMino-5-nitrophthalodinitrile is also utilized in the synthesis of biologically active compounds, which have the potential to interact with biological systems and exhibit various pharmacological effects. Its presence in these compounds can contribute to their biological activity and therapeutic applications.
Used in Pigment Industry:
4-aMino-5-nitrophthalodinitrile is used in the synthesis of novel fully conjugated phenanthroline-appended phthalocyanine. 4-aMino-5-nitrophthalodinitrile has been shown to be effective in the industrial manufacture of blue and green pigments, offering new possibilities for colorants in various industries, such as paints, coatings, and plastics.

Check Digit Verification of cas no

The CAS Registry Mumber 79319-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,1 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79319-38:
(7*7)+(6*9)+(5*3)+(4*1)+(3*9)+(2*3)+(1*8)=163
163 % 10 = 3
So 79319-38-3 is a valid CAS Registry Number.

79319-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-5-nitrophthalodinitrile

1.2 Other means of identification

Product number -
Other names 4-Amino-5-nitrophthalonitrile

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:79319-38-3 SDS

79319-38-3Relevant academic research and scientific papers

Synthesis of phthalonitriles using a palladium catalyst

Iqbal, Zafar,Lyubimtsev, Alexey,Hanack, Michael

experimental part, p. 2287 - 2290 (2009/05/07)

An easy synthetic method to obtain phthalonitriles from o-dibromobenzenes under mild conditions in high yields using Zn(CN)2 and a catalytic amount of tris(dibenzylideneacetone)dipalladium and 1,1′- bis(diphenylphosphino)ferrocene is described. Georg Thieme Verlag Stuttgart.

A novel fully conjugated phenanthroline-appended phthalocyanine: Synthesis and characterisation

Rusanova, Julia,Pilkington, Melanie,Decurtins, Silvio

, p. 2236 - 2237 (2007/10/03)

The synthetic route to a new fully conjugated phenanthroline appended phthalocyanine is described. This compound has been fully characterised by elemental analysis, UV-VIS, IR, MS and 1H NMR spectroscopy.

Nucleophilic substitution in naphthalodinitrile: II. Synthesis and properties of 4-amino-5-nitrophthalodinitrile and its n-acyl derivatives

Zharnikova

, p. 1791 - 1792 (2007/10/03)

Ammonia was reacted with 4-bromo-5-nitrophthalodinitrile in DMF to obtain 4-amino-5-nitrophthalodinitrile. The product was acylated with acetic anhydride and benzoyl chloride.

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