Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2423-73-6

Post Buying Request

2423-73-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2423-73-6 Usage

Description

4-Nitro-2,6-diphenylphenol is an organic compound that is characterized by its ability to react with nitrogen dioxide in a benzene solution, resulting in the formation of C2-epimeric 2,6-dihydroxy-4,5-dinitrocyclohex-3-enones. This chemical property makes it a potentially useful compound in various industrial applications.

Uses

Used in Chemical Synthesis:
4-Nitro-2,6-diphenylphenol is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity with nitrogen dioxide in benzene solution allows for the creation of C2-epimeric 2,6-dihydroxy-4,5-dinitrocyclohex-3-enones, which can be further utilized in the development of other chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Nitro-2,6-diphenylphenol can be used as a starting material for the development of new drugs. Its unique chemical properties may contribute to the creation of novel therapeutic agents with potential applications in various medical fields.
Used in Research and Development:
4-Nitro-2,6-diphenylphenol can also be employed in research and development settings, where its chemical properties can be further explored and harnessed for the creation of new materials, compounds, or processes. This may lead to advancements in various scientific and industrial fields.
Used in Material Science:
In the field of material science, 4-Nitro-2,6-diphenylphenol may be utilized in the development of new materials with specific properties. Its ability to react with nitrogen dioxide and form C2-epimeric 2,6-dihydroxy-4,5-dinitrocyclohex-3-enones could be leveraged to create materials with unique characteristics, such as enhanced stability, reactivity, or other desirable attributes.

Check Digit Verification of cas no

The CAS Registry Mumber 2423-73-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2423-73:
(6*2)+(5*4)+(4*2)+(3*3)+(2*7)+(1*3)=66
66 % 10 = 6
So 2423-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H13NO3/c20-18-16(13-7-3-1-4-8-13)11-15(19(21)22)12-17(18)14-9-5-2-6-10-14/h1-12,20H

2423-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitro-2,6-diphenylphenol

1.2 Other means of identification

Product number -
Other names 5-Nitro-2-oxy-1.3-diphenyl-benzol

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:2423-73-6 SDS

2423-73-6Upstream product

2423-73-6Relevant articles and documents

Diastereoselective synthesis of [1]rotaxanesviaan active metal template strategy

Pairault, No?l,Bessaguet, Adrien,Barat, Romain,Frédéric, Lucas,Pieters, Grégory,Crassous, Jeanne,Opalinski, Isabelle,Papot, Sébastien

, p. 2521 - 2526 (2021/03/01)

Despite the impressive number of interlocked molecules described in the literature over the past 30 years, only a few stereoselective syntheses of mechanically chiral rotaxanes have been reported so far. In this study, we present the first diastereoselective synthesis of mechanically planar chiral [1]rotaxanes, that has been achieved using the active template Cu-mediated alkyne-azide cycloaddition reaction. This synthetic method has been applied to the preparation of a [1]rotaxane bearing a labile stopper that can then be substituted without disruption of the mechanical bond. This approach paves the way for the synthesis of a wide variety of mechanically planar chiral [1]rotaxanes, hence allowing the study of the properties and potential applications of this class of interlocked molecular architectures.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2423-73-6