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4-[(2-methylphenyl)hydrazono]cyclohexa-2,5-dien-1-one is a complex organic compound with the molecular formula C14H15N2O. It is characterized by a cyclohexa-2,5-dien-1-one core, which is a six-membered ring with two double bonds at positions 2 and 5, and a carbonyl group at position 1. The molecule also features a hydrazone functional group attached to the 4-position, which is formed by the condensation of a hydrazine with a carbonyl group. Specifically, the hydrazone is derived from 2-methylphenyl, indicating the presence of a methyl group attached to the phenyl ring. 4-[(2-methylphenyl)hydrazono]cyclohexa-2,5-dien-1-one is likely to be used in chemical research and synthesis due to its unique structure and potential reactivity.

6676-95-5

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6676-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6676-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,7 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6676-95:
(6*6)+(5*6)+(4*7)+(3*6)+(2*9)+(1*5)=135
135 % 10 = 5
So 6676-95-5 is a valid CAS Registry Number.

6676-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2-methylphenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-o-Tolylazo-phenol

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:6676-95-5 SDS

6676-95-5Relevant academic research and scientific papers

The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors

Akwi, Faith M.,Watts, Paul

, p. 1987 - 2004 (2016/10/05)

In this paper, a micro-fluidic optimized process for the continuous flow synthesis of azo compounds is presented. The continuous flow synthesis of Sudan II azo dye was used as a model reaction for the study. At found optimal azo coupling reaction temperature and pH an investigation of the optimum flow rates of the reactants for the diazotization and azo coupling reactions in Little Things Factory-MS microreactors was performed. A conversion of 98% was achieved in approximately 2.4 minutes and a small library of azo compounds was thus generated under these reaction conditions from couplers with aminated or hydroxylated aromatic systems. The scaled up synthesis of these compounds in PTFE tubing (i.d. 1.5 mm) was also investigated, where good reaction conversions ranging between 66-91% were attained.

Modified clays as efficient acid-base catalyst systems for diazotization and diazocoupling reactions

Bahulayan, Damodaran,John, Litka,Lalithambika, Malathy

, p. 863 - 869 (2007/10/03)

Diazotization and diazocoupling reactions of aniline and its substituted derivatives with phenol and other aromatic amines over ecofriendly clay catalysts is described. This inexpensive, non-corrosive and reusable catalysts were found to exhibit bifunctional catalytic properties for these reactions. No considerable decrease in the efficiency of the catalysts were observed after five cycles of operation. The new method totally avoids the use of acids and alkalies.

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