Welcome to LookChem.com Sign In|Join Free
  • or
1,4-Naphthalenedione, mono[(4-methoxyphenyl)hydrazone], also known as 1,4-naphthoquinone mono(4-methoxyphenylhydrazone), is a chemical compound with the molecular formula C17H16N2O3. It is a derivative of 1,4-naphthoquinone, which is a type of quinone, and features a hydrazone functional group attached to the 4-methoxyphenyl moiety. 1,4-Naphthalenedione, mono[(4-methoxyphenyl)hydrazone] is characterized by its yellow crystalline appearance and is soluble in common organic solvents. It is primarily used in organic synthesis and as a reagent in chemical research, particularly in the study of redox reactions and the formation of hydrazone derivatives. The compound's structure and properties make it a valuable tool in the exploration of chemical reactions and the development of new synthetic methods.

32159-06-1

Post Buying Request

32159-06-1 Suppliers

Recommended suppliers

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

32159-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32159-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32159-06:
(7*3)+(6*2)+(5*1)+(4*5)+(3*9)+(2*0)+(1*6)=91
91 % 10 = 1
So 32159-06-1 is a valid CAS Registry Number.

32159-06-1SDS

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 1,4-Naphthochinonyl-(4-methoxyphenylhydrazon)

1.2 Other means of identification

Product number -
Other names 1,4-Naphthochinon-N-p-methoxyphenylhydrazon

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:32159-06-1 SDS

32159-06-1Downstream Products

32159-06-1Relevant academic research and scientific papers

Photooxidation of Arylazo-Naphtholes with Singlet Oxygen

Becker, H. G. O.,Franze, J.

, p. 957 - 964 (2007/10/02)

The reaction of p-substituted 4-arylazo-1-naphtholes 1 and 1-arylazo-2-naphtholes 5 with singlet oxygen (produced by methylene blue-sensitized photolysis) has been studied spectroscopically in methanol as a solvent.The rate constants of dye bleaching are the same, irrespective whether the extinctions of the azo or the hydrazone forms of the tautomeric systems are measured.Both reaction series 1 and 5 afford linear Hammett plots, which is discussed in the light of the azo-hydrazone equilibrium of the dyes and an "ene" mechanism of the reaction with singlet oxygen.It could be shown by short-time spectroscopy that the azo-hydrazone isomerization proceeds much faster than the attack of singlet oxygen on the hydrazone form, which explains all observed facts.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 32159-06-1